Nadolol

Product NDC

60687-324

11-digit product format

606870324

Labeler code

60687

Product ID

60687-324_7017ec2a-396f-771d-e053-2991aa0ae9ee

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Nadolol

Dosage form

TABLET

Route

ORAL

Labeler

American Health Packaging

Application

ANDA203455

Marketing category

ANDA

Marketing start

2017-04-19

Marketing end

2019-03-31

Substance

NADOLOL

Active strength

80 mg/1

Pharmacologic classes

Adrenergic beta

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record