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Cholestyramine - 0185-0940-98 - (Cholestyramine)

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Drug Information of Cholestyramine

Product NDC: 0185-0940
Proprietary Name: Cholestyramine
Non Proprietary Name: Cholestyramine
Active Ingredient(s): 4    g/9g & nbsp;   Cholestyramine
Administration Route(s): ORAL
Dosage Form(s): POWDER, FOR SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Cholestyramine

Product NDC: 0185-0940
Labeler Name: Eon Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074557
Marketing Category: ANDA
Start Marketing Date: 19960815

Package Information of Cholestyramine

Package NDC: 0185-0940-98
Package Description: 60 POUCH in 1 CARTON (0185-0940-98) > 9 g in 1 POUCH

NDC Information of Cholestyramine

NDC Code 0185-0940-98
Proprietary Name Cholestyramine
Package Description 60 POUCH in 1 CARTON (0185-0940-98) > 9 g in 1 POUCH
Product NDC 0185-0940
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cholestyramine
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 19960815
Marketing Category Name ANDA
Labeler Name Eon Labs, Inc.
Substance Name CHOLESTYRAMINE
Strength Number 4
Strength Unit g/9g
Pharmaceutical Classes Bile Acid Sequestrant [EPC],Bile-acid Binding Activity [MoA]

Complete Information of Cholestyramine


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