Carp (Page 3 of 3)

HOW SUPPLIED

Allergenic extracts are supplied with units listed as: Weight/volume (W/V), Protein Nitrogen Units (PNU/ml), Allergy Units (AU/ml) or Bioequivalent Allergy Units (BAU/ml).

Sizes:

Diagnostic Scratch: 5 ml dropper application vials

Diagnostic Intradermal: 5 ml or 10 ml vials.

Therapeutic Allergens: 5 ml, 10 ml, 50 ml multiple dose vials.

STORAGE

The expiration date of allergen extracts is listed on the container label. Store extracts upon arrival at 2° to 8°C and keep them in this range during office use.

WARRANTY: We warrant that this product was prepared and tested according to the standards of the FDA and is true to label. Because of biological differences in individuals and because allergenic extracts are manufactured to be potent and because we have no control over the conditions of use, we cannot and do not warrant either a good effect or against an ill effect following use.

REFERENCES

1 Jacobs, Robert L., Geoffrey W.Rake,Jr., et.al. Potentiated Anaphylaxis in Patients with Drug-induced Beta-adrenergic Blockade. J.Allergy & Clin. Immunol., 68(2): 125-127. August 1981.

2 Ishizaka,K.: Cellular Events in the IgE Antibody Response. Adv. in Immuno. 23:50-75, 1976.

3. Lockey, R.F., Bukantz, S.C., Allergen Immunotherapy. New York,NY: Marcel Dekker Inc., 1991.

4. Reid,M.J., Lockey,R.F., Turkeltaub,P.C., Platts-Mills,T.A.E., Survey of fatalities from skin testing and immunotherapy 1985-1989. Journal of Allergy Clin. Immunol. 92 (1): 6-15, July 1993.

5. Murray, A.B., Ferguson, A., Morrison, B., The frequency and severity of cat allergy vs dog allergy in atopic children. J. Allergy Clin. Immunolo: 72, 145-9, 1983.

6. Lockey, R.F., Bukantz, S.C., Allergen Immunotherapy. New York,NY: Marcel Dekker Inc., 1991.

CONTAINER LABELING

5 mL Stock Intradermal
(click image for full-size original)
5 mL Stock Scratch
(click image for full-size original)
Stock Concentrate Small Label
(click image for full-size original)
Stock Concentrate Large Label
(click image for full-size original)
CARP carp injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1197
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
COMMON CARP (COMMON CARP) COMMON CARP 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
WATER
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-1197-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-1197-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-1197-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-1197-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
CLAM clam injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1201
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CLAM (CLAM) CLAM 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
WATER
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-1201-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-1201-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-1201-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-1201-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
CODFISH codfish injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1205
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CODFISH (CODFISH) CODFISH 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
WATER
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-1205-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-1205-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-1205-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-1205-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
CRAB crab injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1209
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CRAB (CRAB) CRAB 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
WATER
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-1209-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-1209-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-1209-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-1209-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
FLOUNDER flounder injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1213
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
FLOUNDER (FLOUNDER) FLOUNDER 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
WATER
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-1213-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-1213-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-1213-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-1213-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
HADDOCK haddock injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1217
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HADDOCK (HADDOCK) HADDOCK 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
WATER
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-1217-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-1217-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-1217-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-1217-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
HALIBUT halibut injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1221
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PACIFIC HALIBUT (PACIFIC HALIBUT) PACIFIC HALIBUT 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
WATER
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-1221-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-1221-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-1221-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-1221-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
HERRING herring injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1225
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HERRING (HERRING) HERRING 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
WATER
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-1225-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-1225-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-1225-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-1225-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
LOBSTER lobster injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1229
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LOBSTER (LOBSTER) LOBSTER 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
WATER
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-1229-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-1229-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-1229-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-1229-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
MACKEREL mackerel injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1233
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MACKEREL (MACKEREL) MACKEREL 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
WATER
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-1233-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-1233-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-1233-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-1233-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
OYSTER oyster injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1237
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
OYSTER (OYSTER) OYSTER 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
WATER
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-1237-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-1237-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-1237-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-1237-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
RED SNAPPER red snapper injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1245
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RED SNAPPER (RED SNAPPER) RED SNAPPER 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
WATER
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-1245-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-1245-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-1245-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-1245-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
SALMON salmon injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1249
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ATLANTIC SALMON (ATLANTIC SALMON) ATLANTIC SALMON 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
WATER
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-1249-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-1249-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-1249-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-1249-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
SARDINE sardine injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1253
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
EUROPEAN PILCHARD (EUROPEAN PILCHARD) EUROPEAN PILCHARD 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
WATER
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-1253-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-1253-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-1253-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-1253-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
SCALLOP scallop injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1257
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SCALLOP (SCALLOP) SCALLOP 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
WATER
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-1257-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-1257-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-1257-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-1257-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
SHRIMP shrimp injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1261
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SHRIMP (SHRIMP) SHRIMP 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
WATER
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-1261-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-1261-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-1261-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-1261-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
SWORD FISH sword fish injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1269
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SWORDFISH (SWORDFISH) SWORDFISH 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
WATER
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-1269-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-1269-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-1269-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-1269-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
TROUT trout injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1273
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TROUT (TROUT) TROUT 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
WATER
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-1273-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-1273-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-1273-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-1273-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
TUNA FISH tuna fish injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1277
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TUNA (TUNA) TUNA 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
WATER
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-1277-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-1277-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-1277-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-1277-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
WHITE FISH white fish injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1281
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
WHITE FISH (WHITE FISH) WHITE FISH 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
WATER
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-1281-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-1281-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-1281-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-1281-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
PIKE pike injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1241
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
NORTHERN PIKE (NORTHERN PIKE) NORTHERN PIKE 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-1241-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-1241-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-1241-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-1241-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
SMELT smelt injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1265
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SMELT (SMELT) SMELT 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-1265-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-1265-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-1265-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-1265-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
Labeler — Nelco Laboratories, Inc. (054980867)
Registrant — Nelco Laboratories, Inc. (054980867)
Establishment
Name Address ID/FEI Operations
Nelco Laboratories, Inc. 054980867 manufacture

Revised: 12/2009 Nelco Laboratories, Inc.

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