Propranolol Hydrochloride

Product NDC

50111-467

11-digit product format

501110467

Labeler code

50111

Product ID

50111-467_f3e1c898-5846-4434-b220-0392e586f790

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Propranolol Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Teva Pharmaceuticals USA,

Application

ANDA071972

Marketing category

ANDA

Marketing start

1990-09-30

Marketing end

2019-03-31

Substance

PROPRANOLOL HYD

Active strength

10 mg/1

Pharmacologic classes

Adrenergic beta

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record