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Last Updated: November 21, 2024

Details for New Drug Application (NDA): 071922

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NDA 071922 describes METHYLDOPA AND HYDROCHLOROTHIAZIDE, which is a drug marketed by Chartwell Rx, Dava Pharms Inc, Ivax Sub Teva Pharms, Parke Davis, Purepac Pharm, Rising, Sandoz, Strides Pharma, Teva, and Watson Labs, and is included in forty-three NDAs. Additional details are available on the METHYLDOPA AND HYDROCHLOROTHIAZIDE profile page.

The generic ingredient in METHYLDOPA AND HYDROCHLOROTHIAZIDE is hydrochlorothiazide; methyldopa. There are thirty-two drug master file entries for this compound. Additional details are available on the hydrochlorothiazide; methyldopa profile page.

Summary for 071922

Tradename:	METHYLDOPA AND HYDROCHLOROTHIAZIDE
Applicant:	Watson Labs
Ingredient:	hydrochlorothiazide; methyldopa
Patents:	0

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	TABLET;ORAL			Strength	30MG;500MG
Approval Date:	Aug 29, 1988	TE:		RLD:	No

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