Details for New Drug Application (NDA): 017442

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NDA 017442 describes MINIPRESS, which is a drug marketed by Pfizer and is included in two NDAs. It is available from three suppliers. Additional details are available on the MINIPRESS profile page.

The generic ingredient in MINIPRESS is prazosin hydrochloride. There are seventeen drug master file entries for this compound. Thirty suppliers are listed for this compound. Additional details are available on the prazosin hydrochloride profile page.

Summary for 017442

Tradename:	MINIPRESS
Applicant:	Pfizer
Ingredient:	prazosin hydrochloride
Patents:	0

Medical Subject Heading (MeSH) Categories for 017442

Adrenergic alpha-1 Receptor Antagonists
Antihypertensive Agents

Suppliers and Packaging for NDA: 017442

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
MINIPRESS	prazosin hydrochloride	CAPSULE;ORAL	017442	NDA AUTHORIZED GENERIC	Greenstone LLC	59762-5310	59762-5310-1	90 CAPSULE in 1 BOTTLE (59762-5310-1)
MINIPRESS	prazosin hydrochloride	CAPSULE;ORAL	017442	NDA AUTHORIZED GENERIC	Greenstone LLC	59762-5320	59762-5320-1	90 CAPSULE in 1 BOTTLE (59762-5320-1)

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	CAPSULE;ORAL			Strength	EQ 5MG BASE
Approval Date:	Approved Prior to Jan 1, 1982	TE:	AB	RLD:	Yes

Profile for product number 002

Active Rx/OTC/Discontinued:	RX	Dosage:	CAPSULE;ORAL			Strength	EQ 1MG BASE
Approval Date:	Approved Prior to Jan 1, 1982	TE:	AB	RLD:	Yes

Profile for product number 003

Active Rx/OTC/Discontinued:	RX	Dosage:	CAPSULE;ORAL			Strength	EQ 2MG BASE
Approval Date:	Approved Prior to Jan 1, 1982	TE:	AB	RLD:	Yes

Expired US Patents for NDA 017442

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Applicant	Tradename	Generic Name	Dosage	NDA	Approval Date	Patent No.	Patent Expiration
Pfizer	MINIPRESS	prazosin hydrochloride	CAPSULE;ORAL	017442-001	Approved Prior to Jan 1, 1982	⤷ Sign Up	⤷ Sign Up
Pfizer	MINIPRESS	prazosin hydrochloride	CAPSULE;ORAL	017442-002	Approved Prior to Jan 1, 1982	⤷ Sign Up	⤷ Sign Up
Pfizer	MINIPRESS	prazosin hydrochloride	CAPSULE;ORAL	017442-002	Approved Prior to Jan 1, 1982	⤷ Sign Up	⤷ Sign Up
>Applicant	>Tradename	>Generic Name	>Dosage	>NDA	>Approval Date	>Patent No.	>Patent Expiration

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