Carvedilol

Product NDC

68084-865

11-digit product format

680840865

Labeler code

68084

Product ID

68084-865_81a2c395-d5ed-6bda-e053-2991aa0aeda5

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Carvedilol

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

American Health Packaging

Application

ANDA077614

Marketing category

ANDA

Marketing start

2015-03-20

Marketing end

2019-12-31

Substance

CARVEDILOL

Active strength

13 mg/1

Pharmacologic classes

Adrenergic alpha-Antagonists [MoA],Adrenergic beta1-Antagonists [MoA],Adrenergic beta2-Antagonists [MoA],alpha-Adrenergic Blocker [EPC],beta-Adrenergic Blocker [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record