HydrALAZINE Hydrochloride

Product NDC

70518-1403

11-digit product format

705181403

Labeler code

70518

Product ID

70518-1403_92bcb0d9-12bb-579a-e053-2a95a90abe2d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

HydrALAZINE Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA200770

Marketing category

ANDA

Marketing start

2018-09-07

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

2020-12-31

Current FDA listing

Historical FDA.report record