Drugs@FDA: FDA-Approved Drugs

Home | Previous Page

New Drug Application (NDA): 017442
Company: PFIZER

Products on NDA 17442

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
MINIPRESS	PRAZOSIN HYDROCHLORIDE	EQ 5MG BASE	CAPSULE;ORAL	Prescription	AB	Yes	No
MINIPRESS	PRAZOSIN HYDROCHLORIDE	EQ 1MG BASE	CAPSULE;ORAL	Prescription	AB	Yes	No
MINIPRESS	PRAZOSIN HYDROCHLORIDE	EQ 2MG BASE	CAPSULE;ORAL	Prescription	AB	Yes	Yes

Labels for NDA 017442

Action Date	Submission	Supplement Categories or Approval Type	Letters, Reviews, Labels, Patient Package Insert	Note	Url
02/27/2015	SUPPL-43	Labeling-Package Insert	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2015/017442 s043lbl.pdf
11/04/2013	SUPPL-41	Labeling-Package Insert	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2013/017442s041lbl.pdf
07/10/2009	SUPPL-35	Labeling	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2009/017442s035lbl.pdf
04/06/2009	SUPPL-33	Labeling	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2009/017442s033lbl.pdf