Propranolol Hydrochloride

Product NDC

70518-2444

11-digit product format

705182444

Labeler code

70518

Product ID

70518-2444_98232e8a-f6d2-bd8a-e053-2a95a90a5232

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Propranolol Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA070178

Marketing category

ANDA

Marketing start

2019-11-22

Marketing end

0000-00-00

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

2020-12-31

Current FDA listing

Historical FDA.report record