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 Action	Bile-acid Binding Activity

Medical Subject Heading (MeSH) Categories for 020222

Anion Exchange Resins
Hypolipidemic Agents
Sequestering Agents

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:	RX	Dosage:	TABLET;ORAL			Strength	1GM
Approval Date:	Jul 19, 1994	TE:	AB	RLD:	Yes

Expired US Patents for NDA 020222

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Applicant	Tradename	Generic Name	Dosage	NDA	Approval Date	Patent No.	Patent Expiration
Pfizer	COLESTID	colestipol hydrochloride	TABLET;ORAL	020222-001	Jul 19, 1994	5,490,987	⤷ Subscribe
>Applicant	>Tradename	>Generic Name	>Dosage	>NDA	>Approval Date	>Patent No.	>Patent Expiration

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