Last Updated: September 29, 2026

Details for New Drug Application (NDA): 071641

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NDA 071641 describes MECLOFENAMATE SODIUM, which is a drug marketed by Am Therap, Ani Pharms, Barr, Chartwell Rx, Mylan, Par Pharm, Usl Pharma, Vitarine, and Watson Labs, and is included in eighteen NDAs. It is available from one supplier. Additional details are available on the MECLOFENAMATE SODIUM profile page.

The generic ingredient in MECLOFENAMATE SODIUM is meclofenamate sodium. There is one drug master file entry for this compound. One supplier is listed for this compound. Additional details are available on the meclofenamate sodium profile page.

Summary for 071641

Tradename:	MECLOFENAMATE SODIUM
Applicant:	Watson Labs
Ingredient:	meclofenamate sodium
Patents:	0

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	CAPSULE;ORAL			Strength	EQ 100MG BASE
Approval Date:	Aug 11, 1987	TE:		RLD:	No

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