Albuterol

Product NDC

51079-658

11-digit product format

510790658

Labeler code

51079

Product ID

51079-658_7b1abf21-d13f-78c2-e053-2a91aa0ace48

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

albuterol

Dosage form

TABLET

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

ANDA072894

Marketing category

ANDA

Marketing start

1997-04-29

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

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record