Hydralazine Hydrochloride

Product NDC

63739-127

11-digit product format

637390127

Labeler code

63739

Product ID

63739-127_b3d69d05-ff61-52f1-e053-2995a90ac23a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Hydralazine Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

McKesson Corporation dba SKY Packaging

Application

ANDA088468

Marketing category

ANDA

Marketing start

1990-09-30

Marketing end

2020-11-30

Substance

HYDRALAZINE HYDROCHLORIDE

Active strength

50 mg/1

Pharmacologic classes

Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record