Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 017986
Company: PFIZER

Products on NDA 017986

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
MINIZIDE	POLYTHIAZIDE; PRAZOSIN HYDROCHLORIDE	0.5MG;EQ 1MG BASE	CAPSULE;ORAL	Discontinued	None	No	No
MINIZIDE	POLYTHIAZIDE; PRAZOSIN HYDROCHLORIDE	0.5MG;EQ 2MG BASE	CAPSULE;ORAL	Discontinued	None	No	No
MINIZIDE	POLYTHIAZIDE; PRAZOSIN HYDROCHLORIDE	0.5MG;EQ 5MG BASE	CAPSULE;ORAL	Discontinued	None	No	No

Approval Date(s) and History, Letters, Labels, Reviews for NDA 017986

Original Approvals or Tentative Approvals

Action Date	Submission	Action Type	Submission Classification	Review Priority; Orphan Status	Letters, Reviews, Labels, Patient Package Insert	Notes	Url
06/13/1980	ORIG-1	Approval	Type 4 - New Combination	STANDARD		Label is not available on this site.

Supplements

Action Date	Submission	Supplement Categories or Approval Type	Letters, Reviews, Labels, Patient Package Insert	Note	Url
05/10/1994	SUPPL-12	Manufacturing (CMC)		Label is not available on this site.
06/26/1992	SUPPL-11	Manufacturing (CMC)		Label is not available on this site.
05/01/1989	SUPPL-10	Labeling		Label is not available on this site.
02/26/1985	SUPPL-9	Labeling		Label is not available on this site.
08/13/1984	SUPPL-8	Labeling		Label is not available on this site.
04/06/1984	SUPPL-7	Manufacturing (CMC)-Packaging		Label is not available on this site.
08/01/1984	SUPPL-6	Manufacturing (CMC)-Packaging		Label is not available on this site.
08/22/1984	SUPPL-5	Manufacturing (CMC)-Packaging		Label is not available on this site.
07/02/1982	SUPPL-4	Manufacturing (CMC)-Packaging		Label is not available on this site.
07/31/1981	SUPPL-3	Manufacturing (CMC)-Packaging		Label is not available on this site.
12/01/1981	SUPPL-2	Manufacturing (CMC)		Label is not available on this site.
02/19/1981	SUPPL-1	Labeling		Label is not available on this site.