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Last Updated: November 22, 2024

Details for New Drug Application (NDA): 020222


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NDA 020222 describes COLESTID, which is a drug marketed by Pfizer and is included in two NDAs. It is available from two suppliers. Additional details are available on the COLESTID profile page.

The generic ingredient in COLESTID is colestipol hydrochloride. There are two drug master file entries for this compound. Eight suppliers are listed for this compound. Additional details are available on the colestipol hydrochloride profile page.
Summary for 020222
Tradename:COLESTID
Applicant:Pfizer
Ingredient:colestipol hydrochloride
Patents:0
Pharmacology for NDA: 020222
Mechanism of ActionBile-acid Binding Activity
Medical Subject Heading (MeSH) Categories for 020222
Suppliers and Packaging for NDA: 020222
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
COLESTID colestipol hydrochloride TABLET;ORAL 020222 NDA Pharmacia & Upjohn Company LLC 0009-0450 0009-0450-03 120 TABLET in 1 BOTTLE (0009-0450-03)
COLESTID colestipol hydrochloride TABLET;ORAL 020222 NDA AUTHORIZED GENERIC Greenstone LLC 59762-0450 59762-0450-1 120 TABLET in 1 BOTTLE (59762-0450-1)

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength1GM
Approval Date:Jul 19, 1994TE:ABRLD:Yes

Expired US Patents for NDA 020222

Applicant Tradename Generic Name Dosage NDA Approval Date Patent No. Patent Expiration
Pfizer COLESTID colestipol hydrochloride TABLET;ORAL 020222-001 Jul 19, 1994 ⤷  Sign Up ⤷  Sign Up
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >Patent No. >Patent Expiration

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