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Last Updated: December 30, 2025

Details for New Drug Application (NDA): 040359

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NDA 040359 describes ESTROPIPATE, which is a drug marketed by Barr, Duramed Pharms Barr, Pharmobedient, Watson Labs, and Watson Labs Teva, and is included in seven NDAs. Additional details are available on the ESTROPIPATE profile page.

The generic ingredient in ESTROPIPATE is estropipate. There are two drug master file entries for this compound. Additional details are available on the estropipate profile page.

Summary for 040359

Tradename:	ESTROPIPATE
Applicant:	Pharmobedient
Ingredient:	estropipate
Patents:	0

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	TABLET;ORAL			Strength	0.75MG
Approval Date:	Aug 26, 1999	TE:		RLD:	No

Profile for product number 002

Active Rx/OTC/Discontinued:	DISCN	Dosage:	TABLET;ORAL			Strength	1.5MG
Approval Date:	Aug 26, 1999	TE:		RLD:	No

Profile for product number 003

Active Rx/OTC/Discontinued:	DISCN	Dosage:	TABLET;ORAL			Strength	3MG
Approval Date:	Aug 26, 1999	TE:		RLD:	No

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