Propranolol Hydrochloride

Product NDC

50436-4315

11-digit product format

504364315

Labeler code

50436

Product ID

50436-4315_d266a2f3-a7bb-4837-9ec2-d4be17f4373d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Propranolol Hydrochloride

Dosage form

CAPSULE, EXTENDED RELEASE

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA078494

Marketing category

ANDA

Marketing start

2007-08-10

Marketing end

0000-00-00

Substance

PROPRANOLOL HYDROCHLORIDE

Active strength

60 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record