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Colestipol Hydrochloride - 59762-0450-1 - (Colestipol Hydrochloride)

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Drug Information of Colestipol Hydrochloride

Product NDC: 59762-0450
Proprietary Name: Colestipol Hydrochloride
Non Proprietary Name: Colestipol Hydrochloride
Active Ingredient(s): 1    g/1 & nbsp;   Colestipol Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Colestipol Hydrochloride

Product NDC: 59762-0450
Labeler Name: Greenstone LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020222
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 19940719

Package Information of Colestipol Hydrochloride

Package NDC: 59762-0450-1
Package Description: 120 TABLET in 1 BOTTLE (59762-0450-1)

NDC Information of Colestipol Hydrochloride

NDC Code 59762-0450-1
Proprietary Name Colestipol Hydrochloride
Package Description 120 TABLET in 1 BOTTLE (59762-0450-1)
Product NDC 59762-0450
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Colestipol Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19940719
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Greenstone LLC
Substance Name COLESTIPOL HYDROCHLORIDE
Strength Number 1
Strength Unit g/1
Pharmaceutical Classes Bile Acid Sequestrant [EPC],Bile-acid Binding Activity [MoA]

Complete Information of Colestipol Hydrochloride


General Information