Hydralazine Hydrochloride

Product NDC

55154-4179

11-digit product format

551544179

Labeler code

55154

Product ID

55154-4179_783f05ed-eba9-46f3-af20-9f51daaac786

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Hydralazine Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Cardinal Health

Application

ANDA086242

Marketing category

ANDA

Marketing start

2007-04-06

Marketing end

0000-00-00

Substance

HYDRALAZINE HYDROCHLORIDE

Active strength

10 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