Bisoprolol Fumarate and Hydrochlorothiazide

Product NDC

63629-4072

11-digit product format

636294072

Labeler code

63629

Product ID

63629-4072_8b4d4bd5-02f5-4a14-b6b2-131485514bed

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Bisoprolol Fumarate and Hydrochlorothiazide

Dosage form

TABLET, COATED

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA075579

Marketing category

ANDA

Marketing start

2000-09-25

Marketing end

0000-00-00

Substance

BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE

Active strength

5 mg/1; mg/1

Pharmacologic classes

Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record