Last Updated: September 24, 2026

Details for New Drug Application (NDA): 018932

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NDA 018932 describes REVIA, which is a drug marketed by Teva Womens and is included in one NDA. Additional details are available on the REVIA profile page.

The generic ingredient in REVIA is naltrexone hydrochloride. There is one drug master file entry for this compound. Twenty-one suppliers are listed for this compound. Additional details are available on the naltrexone hydrochloride profile page.

Summary for 018932

Tradename:	REVIA
Applicant:	Teva Womens
Ingredient:	naltrexone hydrochloride
Patents:	0

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	TABLET;ORAL			Strength	50MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons
Approval Date:	Nov 20, 1984	TE:		RLD:	Yes

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