Propranolol Hydrochloride

Product NDC

50111-471

11-digit product format

501110471

Labeler code

50111

Product ID

50111-471_f3e1c898-5846-4434-b220-0392e586f790

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Propranolol Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Teva Pharmaceuticals USA, Inc.

Application

ANDA071976

Marketing category

ANDA

Marketing start

1990-09-30

Marketing end

2019-04-30

Substance

PROPRANOLOL HYDROCHLORIDE

Active strength

80 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record