albuterol sulfate

Product NDC

63629-2736

11-digit product format

636292736

Labeler code

63629

Product ID

63629-2736_421c0535-c26d-444f-84ce-0b02ccc8b854

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

albuterol sulfate

Dosage form

TABLET

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA072637

Marketing category

ANDA

Marketing start

1989-12-05

Marketing end

0000-00-00

Substance

ALBUTEROL SULFATE

Active strength

4 mg/1

Pharmacologic classes

Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record