Hydralazine Hydrochloride

Product NDC

0615-0532

11-digit product format

006150532

Labeler code

0615

Product ID

0615-0532_1cce9fcb-74f7-4f96-a546-5572b96d4d7c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Hydralazine Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

NCS HealthCare of KY, Inc dba Vangard Labs

Application

ANDA086962

Marketing category

ANDA

Marketing start

1980-02-27

Marketing end

0000-00-00

Substance

HYDRALAZINE HYDROCHLORIDE

Active strength

50 mg/1

Pharmacologic classes

Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record