HydrALAZINE Hydrochloride

Product NDC

59556-008

11-digit product format

595560008

Labeler code

59556

Product ID

59556-008_82d20232-4f22-4220-88da-8f8445d79e30

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

HydrALAZINE Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Strides Pharma Inc

Application

ANDA200770

Marketing category

ANDA

Marketing start

2013-05-04

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