Heparin Sodium (Page 6 of 6)

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL — 10,000 USP Units/mL — 1 mL Container-Carton [25 Multiple Dose Vials]

NDC 63739-964-25 Rx only
HEPARIN
SODIUM INJECTION, USP
10,000 USP Units/mL
1 mL
NOT FOR LOCK FLUSH
For Intravenous or
Subcutaneous use
25 Multiple-Dose Vials
Derived from Porcine Intestinal Mucosa

heparin-fig10
(click image for full-size original)

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL — 50,000 USP Units/5 mL (10,000 USP Units/mL) — 5 mL Container Label

NDC 63739-975-13 Rx only
HEPARIN
SODIUM INJECTION, USP
50,000 USP Units/5 mL
(10,000 USP Units/mL)
For IV or SC use
Multiple Dose Vial 5 mL

NOT FOR LOCK FLUSH

heparin-fig11
(click image for full-size original)

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL — 50,000 USP Units/5 mL (10,000 USP Units/mL) — 5 mL Container-Carton [25 Multiple Dose Vials]

NDC 63739-975-27 Rx only
HEPARIN
SODIUM INJECTION, USP
50,000 USP Units/5 mL
(10,000 USP Units/mL)
5 mL
NOT FOR LOCK FLUSH
For Intravenous or Subcutaneous use
25 Multiple-Dose Vials
Derived from Porcine Intestinal Mucosa

heparin-fig12
(click image for full-size original)

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL — 20,000 USP Units/mL — 1 mL Container Label

NDC 63739-986-11 Rx only
HEPARIN
SODIUM INJECTION, USP
20,000 USP Units/mL
For IV or SC use
Multiple Dose Vial 1 mL

NOT FOR LOCK FLUSH

heparin-fig13
(click image for full-size original)

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL — 20,000 USP Units/mL — 1 mL Container-Carton [25 Multiple Dose Vials]

NDC 63739-986-25 Rx only
HEPARIN
SODIUM INJECTION, USP
20,000 USP Units/mL
1 mL
NOT FOR LOCK FLUSH
For Intravenous or
Subcutaneous use
25 Multiple-Dose Vials
Derived from Porcine Intestinal Mucosa

heparin-fig14
(click image for full-size original)

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL- 2,000 USP Units/2 mL (1,000 USP Units/mL) — 2 mL Container Label

NDC 63739-900-12 Rx only
HEPARIN
SODIUM INJECTION, USP
2,000 USP Units/2 mL
(1,000 USP Units/mL)
For IV or SC use
Preservative Free
Discard unused portion
2 mL Single Dose Vial

NOT FOR LOCK FLUSH

heparin-fig15
(click image for full-size original)

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL- 2,000 USP Units/2 mL (1,000 USP Units/mL) — 2 mL Container-Carton [25 Single Dose Vials]

NDC 63739-900-26 Rx only
HEPARIN
SODIUM INJECTION, USP
2,000 USP Units/2 mL
(1,000 USP Units/mL)
2 mL
NOT FOR LOCK FLUSH
For Intravenous or
Subcutaneous use
Preservative Free
25 Single-Dose Vials Derived from Porcine Intestinal Mucosa

heparin-fig16
(click image for full-size original)

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL- 50,000 USP Units/10 mL (5,000 USP Units/mL) — 10 mL Container Label

NDC 63739-901-14 Rx only
HEPARIN
SODIUM INJECTION, USP
50,000 USP Units/10 mL
(5,000 USP Units/mL)
For IV or SC use
Warning: Contains Benzyl Alcohol
10 mL Multiple Dose Vial NOT FOR LOCK FLUSH

heparin-fig17
(click image for full-size original)

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL- 50,000 USP Units/10 mL (5,000 USP Units/mL) — 10 mL Container-Carton [25 Multiple Dose Vials]

NDC 63739-901-28 Rx only
HEPARIN
SODIUM INJECTION, USP
50,000 USP Units/10 mL
(5,000 USP Units/mL)
10 mL
NOT FOR LOCK FLUSH
Warning: Contains Benzyl Alcohol
For Intravenous or Subcutaneous use
25 Multiple-Dose Vials Derived from Porcine Intestinal Mucosa

heparin-fig18
(click image for full-size original)
HEPARIN SODIUM heparin sodium injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:63739-920
Route of Administration INTRAVENOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HEPARIN SODIUM (HEPARIN) HEPARIN 1000 [USP’U] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE 9 mg in 1 mL
METHYLPARABEN 1.5 mg in 1 mL
PROPYLPARABEN 0.15 mg in 1 mL
WATER
HYDROCHLORIC ACID
SODIUM HYDROXIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:63739-920-25 25 VIAL, MULTI-DOSE in 1 CARTON contains a VIAL, MULTI-DOSE (63739-920-11)
1 NDC:63739-920-11 1 mL in 1 VIAL, MULTI-DOSE This package is contained within the CARTON (63739-920-25)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA202957 06/12/2014
HEPARIN SODIUM heparin sodium injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:63739-931
Route of Administration INTRAVENOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HEPARIN SODIUM (HEPARIN) HEPARIN 1000 [USP’U] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE 9 mg in 1 mL
METHYLPARABEN 1.5 mg in 1 mL
PROPYLPARABEN 0.15 mg in 1 mL
WATER
HYDROCHLORIC ACID
SODIUM HYDROXIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:63739-931-28 25 VIAL, MULTI-DOSE in 1 CARTON contains a VIAL, MULTI-DOSE (63739-931-14)
1 NDC:63739-931-14 10 mL in 1 VIAL, MULTI-DOSE This package is contained within the CARTON (63739-931-28)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA202957 06/12/2014
HEPARIN SODIUM heparin sodium injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:63739-942
Route of Administration INTRAVENOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HEPARIN SODIUM (HEPARIN) HEPARIN 1000 [USP’U] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE 9 mg in 1 mL
METHYLPARABEN 1.5 mg in 1 mL
PROPYLPARABEN 0.15 mg in 1 mL
WATER
HYDROCHLORIC ACID
SODIUM HYDROXIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:63739-942-29 25 VIAL, MULTI-DOSE in 1 CARTON contains a VIAL, MULTI-DOSE (63739-942-15)
1 NDC:63739-942-15 30 mL in 1 VIAL, MULTI-DOSE This package is contained within the CARTON (63739-942-29)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA202957 06/12/2014
HEPARIN SODIUM heparin sodium injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:63739-953
Route of Administration INTRAVENOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HEPARIN SODIUM (HEPARIN) HEPARIN 5000 [USP’U] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE 5 mg in 1 mL
METHYLPARABEN 1.5 mg in 1 mL
PROPYLPARABEN 0.15 mg in 1 mL
WATER
HYDROCHLORIC ACID
SODIUM HYDROXIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:63739-953-25 25 VIAL, MULTI-DOSE in 1 CARTON contains a VIAL, MULTI-DOSE (63739-953-11)
1 NDC:63739-953-11 1 mL in 1 VIAL, MULTI-DOSE This package is contained within the CARTON (63739-953-25)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA202957 06/12/2014
HEPARIN SODIUM heparin sodium injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:63739-964
Route of Administration INTRAVENOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HEPARIN SODIUM (HEPARIN) HEPARIN 10000 [USP’U] in 1 mL
Inactive Ingredients
Ingredient Name Strength
METHYLPARABEN 1.5 mg in 1 mL
PROPYLPARABEN 0.15 mg in 1 mL
WATER
HYDROCHLORIC ACID
SODIUM HYDROXIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:63739-964-25 25 VIAL, MULTI-DOSE in 1 CARTON contains a VIAL, MULTI-DOSE (63739-964-11)
1 NDC:63739-964-11 1 mL in 1 VIAL, MULTI-DOSE This package is contained within the CARTON (63739-964-25)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA203198 06/12/2014
HEPARIN SODIUM heparin sodium injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:63739-975
Route of Administration INTRAVENOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HEPARIN SODIUM (HEPARIN) HEPARIN 10000 [USP’U] in 1 mL
Inactive Ingredients
Ingredient Name Strength
METHYLPARABEN 1.5 mg in 1 mL
PROPYLPARABEN 0.15 mg in 1 mL
WATER
HYDROCHLORIC ACID
SODIUM HYDROXIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:63739-975-27 25 VIAL, MULTI-DOSE in 1 CARTON contains a VIAL, MULTI-DOSE (63739-975-13)
1 NDC:63739-975-13 5 mL in 1 VIAL, MULTI-DOSE This package is contained within the CARTON (63739-975-27)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA203198 06/12/2014
HEPARIN SODIUM heparin sodium injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:63739-986
Route of Administration INTRAVENOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HEPARIN SODIUM (HEPARIN) HEPARIN 20000 [USP’U] in 1 mL
Inactive Ingredients
Ingredient Name Strength
METHYLPARABEN 1.5 mg in 1 mL
PROPYLPARABEN 0.15 mg in 1 mL
WATER
HYDROCHLORIC ACID
SODIUM HYDROXIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:63739-986-25 25 VIAL, MULTI-DOSE in 1 CARTON contains a VIAL, MULTI-DOSE (63739-986-11)
1 NDC:63739-986-11 1 mL in 1 VIAL, MULTI-DOSE This package is contained within the CARTON (63739-986-25)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA203198 06/12/2014
HEPARIN SODIUM heparin sodium injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:63739-900
Route of Administration INTRAVENOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HEPARIN SODIUM (HEPARIN) HEPARIN 1000 [USP’U] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE 9 mg in 1 mL
WATER
HYDROCHLORIC ACID
SODIUM HYDROXIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:63739-900-26 25 VIAL, SINGLE-DOSE in 1 CARTON contains a VIAL, SINGLE-DOSE (63739-900-12)
1 NDC:63739-900-12 2 mL in 1 VIAL, SINGLE-DOSE This package is contained within the CARTON (63739-900-26)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA202732 06/12/2014
HEPARIN SODIUM heparin sodium injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:63739-901
Route of Administration INTRAVENOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HEPARIN SODIUM (HEPARIN) HEPARIN 5000 [USP’U] in 1 mL
Inactive Ingredients
Ingredient Name Strength
BENZYL ALCOHOL 15 mg in 1 mL
SODIUM CHLORIDE 6 mg in 1 mL
WATER
HYDROCHLORIC ACID
SODIUM HYDROXIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:63739-901-28 25 VIAL, MULTI-DOSE in 1 CARTON contains a VIAL, MULTI-DOSE (63739-901-14)
1 NDC:63739-901-14 10 mL in 1 VIAL, MULTI-DOSE This package is contained within the CARTON (63739-901-28)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA202733 06/12/2014
Labeler — McKesson Corporation dba SKY Packaging (140529962)
Establishment
Name Address ID/FEI Operations
Shenzhen Techdow Pharmaceutical Co., Ltd. 527809171 analysis (63739-900), analysis (63739-901), analysis (63739-920), analysis (63739-931), analysis (63739-942), analysis (63739-953), analysis (63739-964), analysis (63739-975), analysis (63739-986), manufacture (63739-900), manufacture (63739-901), manufacture (63739-920), manufacture (63739-931), manufacture (63739-942), manufacture (63739-953), manufacture (63739-964), manufacture (63739-975), manufacture (63739-986)
Establishment
Name Address ID/FEI Operations
Shenzhen Hepalink Pharmaceutical Group Co., Ltd. 547034665 api manufacture (63739-900), api manufacture (63739-901), api manufacture (63739-920), api manufacture (63739-931), api manufacture (63739-942), api manufacture (63739-953), api manufacture (63739-964), api manufacture (63739-975), api manufacture (63739-986)
Establishment
Name Address ID/FEI Operations
Eugia Pharma Specialities Limited 650498244 analysis (63739-900), analysis (63739-901), analysis (63739-920), analysis (63739-931), analysis (63739-942), analysis (63739-953), analysis (63739-964), analysis (63739-975), analysis (63739-986), manufacture (63739-900), manufacture (63739-901), manufacture (63739-920), manufacture (63739-931), manufacture (63739-942), manufacture (63739-953), manufacture (63739-964), manufacture (63739-975), manufacture (63739-986)

Revised: 08/2023 McKesson Corporation dba SKY Packaging

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