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cholestyramine light - 0185-0939-98 - (cholestyramine light)

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Drug Information of cholestyramine light

Product NDC: 0185-0939
Proprietary Name: cholestyramine light
Non Proprietary Name: cholestyramine light
Active Ingredient(s): 4    g/5.7g & 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: 0185-0939
Labeler Name: Eon Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074558
Marketing Category: ANDA
Start Marketing Date: 19941104

Package Information of cholestyramine light

Package NDC: 0185-0939-98
Package Description: 60 POUCH in 1 CARTON (0185-0939-98) > 5.7 g in 1 POUCH

NDC Information of cholestyramine light

NDC Code 0185-0939-98
Proprietary Name cholestyramine light
Package Description 60 POUCH in 1 CARTON (0185-0939-98) > 5.7 g in 1 POUCH
Product NDC 0185-0939
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name cholestyramine light
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 19941104
Marketing Category Name ANDA
Labeler Name Eon Labs, Inc.
Substance Name CHOLESTYRAMINE
Strength Number 4
Strength Unit g/5.7g
Pharmaceutical Classes Bile Acid Sequestrant [EPC],Bile-acid Binding Activity [MoA]

Complete Information of cholestyramine light


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