Hydralazine Hydrochloride

Product NDC

50436-7376

11-digit product format

504367376

Labeler code

50436

Product ID

50436-7376_0ef66670-4c90-4e96-808b-1c082058247c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Hydralazine Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA086242

Marketing category

ANDA

Marketing start

2007-04-06

Marketing end

0000-00-00

Substance

HYDRALAZINE HYDROCHLORIDE

Active strength

25 mg/1

Pharmacologic classes

Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record