Home > National Drug Code (NDC) > CHOLESTYRAMINE LIGHT

CHOLESTYRAMINE LIGHT - 60429-356-21 - (cholestyramine light)

Alphabetical Index


Drug Information of CHOLESTYRAMINE LIGHT

Product NDC: 60429-356
Proprietary Name: CHOLESTYRAMINE LIGHT
Non Proprietary Name: cholestyramine light
Active Ingredient(s): 4    g/5g & nbsp;   cholestyramine light
Administration Route(s): ORAL
Dosage Form(s): POWDER, FOR SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of CHOLESTYRAMINE LIGHT

Product NDC: 60429-356
Labeler Name: Golden State Medical Supply, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077204
Marketing Category: ANDA
Start Marketing Date: 20050915

Package Information of CHOLESTYRAMINE LIGHT

Package NDC: 60429-356-21
Package Description: 210 g in 1 CAN (60429-356-21)

NDC Information of CHOLESTYRAMINE LIGHT

NDC Code 60429-356-21
Proprietary Name CHOLESTYRAMINE LIGHT
Package Description 210 g in 1 CAN (60429-356-21)
Product NDC 60429-356
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name cholestyramine light
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 20050915
Marketing Category Name ANDA
Labeler Name Golden State Medical Supply, Inc.
Substance Name CHOLESTYRAMINE
Strength Number 4
Strength Unit g/5g
Pharmaceutical Classes Bile Acid Sequestrant [EPC],Bile-acid Binding Activity [MoA]

Complete Information of CHOLESTYRAMINE LIGHT


General Information