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Last Updated: December 23, 2024

Details for New Drug Application (NDA): 070830

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NDA 070830 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 070830

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

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	TABLET;ORAL			Strength	25MG;250MG
Approval Date:	Mar 9, 1987	TE:		RLD:	No

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