Nadolol

Product NDC

63629-7483

11-digit product format

636297483

Labeler code

63629

Product ID

63629-7483_3bdbedbd-6666-457e-827e-8901ef894908

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Nadolol

Dosage form

TABLET

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA074501

Marketing category

ANDA

Marketing start

2008-10-01

Marketing end

0000-00-00

Substance

NADOLOL

Active strength

80 mg/1

Pharmacologic classes

Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record