Albuterol Sulfate

Product NDC

24208-347

11-digit product format

242080347

Labeler code

24208

Product ID

24208-347_bffd58d4-3b39-4d2e-8685-facb74fdaa73

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Albuterol Sulfate

Dosage form

SOLUTION

Route

RESPIRATORY (INHALATION)

Labeler

Bausch & Lomb Incorporated

Application

ANDA075050

Marketing category

ANDA

Marketing start

1998-06-18

Marketing end

0000-00-00

Substance

ALBUTEROL SULFATE

Active strength

5 mg/mL

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record