Albuterol Sulfate

Product NDC

68071-4199

11-digit product format

680714199

Labeler code

68071

Product ID

68071-4199_6140f008-7530-1555-e053-2a91aa0ae176

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Albuterol Sulfate

Dosage form

SOLUTION

Route

INTRABRONCHIAL

Labeler

NuCare Pharmaceuticals,Inc.

Application

ANDA077839

Marketing category

ANDA

Marketing start

2010-11-04

Marketing end

0000-00-00

Substance

ALBUTEROL SULFATE

Active strength

3 mg/3mL

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