Nadolol

Product NDC

0093-4237

11-digit product format

000934237

Labeler code

0093

Product ID

0093-4237_af5152c5-3641-4622-9295-02e9ac51b0d5

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Nadolol

Dosage form

TABLET

Route

ORAL

Labeler

Teva Pharmaceuticals USA, Inc.

Application

ANDA074255

Marketing category

ANDA

Marketing start

2008-11-03

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

2020-12-31

Current FDA listing

Historical FDA.report record