CORZIDE

Product NDC

60793-284

11-digit product format

607930284

Labeler code

60793

Product ID

60793-284_634fa33e-798d-49ac-b968-9e8b48fa7239

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

nadolol and bendroflumethiazide

Dosage form

TABLET

Route

ORAL

Labeler

Pfizer Laboratories Div Pfizer Inc

Application

NDA018647

Marketing category

NDA

Marketing start

1983-05-25

Marketing end

2019-10-31

Substance

NADOLOL; BENDROFLUMETHIAZIDE

Active strength

80 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

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record