CARISOPRODOL (Page 5 of 5)

Principal Display Panel

NDC: 70934-663-30

label
(click image for full-size original)
CARISOPRODOL carisoprodol tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:70934-663(NDC:50228-109)
Route of Administration ORAL DEA Schedule CIV
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CARISOPRODOL (CARISOPRODOL) CARISOPRODOL 350 mg
Inactive Ingredients
Ingredient Name Strength
MICROCRYSTALLINE CELLULOSE
LACTOSE MONOHYDRATE
STARCH, CORN
CROSCARMELLOSE SODIUM
POVIDONE, UNSPECIFIED
SILICON DIOXIDE
MAGNESIUM STEARATE
Product Characteristics
Color white Score no score
Shape ROUND Size 12mm
Flavor Imprint Code SG;109
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:70934-663-30 30 TABLET in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA203374 04/10/2020
Labeler — Denton Pharma, Inc. dba Northwind Pharmaceuticals (080355546)
Registrant — Denton Pharma, Inc. dba Northwind Pharmaceuticals (080355546)
Establishment
Name Address ID/FEI Operations
Denton Pharma, Inc. dba Northwind Pharmaceuticals 080355546 repack (70934-663)

Revised: 07/2020 Denton Pharma, Inc. dba Northwind Pharmaceuticals

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