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Product Details for ANDA 202902

CHOLESTYRAMINE LIGHT (CHOLESTYRAMINE)
EQ 4GM RESIN/SCOOPFUL
Marketing Status: Prescription
Active Ingredient: CHOLESTYRAMINE
Proprietary Name: CHOLESTYRAMINE LIGHT
Dosage Form; Route of Administration: POWDER; ORAL
Strength: EQ 4GM RESIN/SCOOPFUL
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A202902
Product Number: 001
Approval Date: Apr 25, 2017
Applicant Holder Full Name: ZYDUS PHARMACEUTICALS USA INC
Marketing Status:  Prescription
Patent and Exclusivity Information

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