Albuterol Sulfate

Product NDC

68788-7390

11-digit product format

687887390

Labeler code

68788

Product ID

68788-7390_b7ebb89d-07f4-4820-8718-bc7930c71ae5

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Albuterol Sulfate

Dosage form

SYRUP

Route

ORAL

Labeler

Preferred Pharmaceuticals Inc.

Application

ANDA074454

Marketing category

ANDA

Marketing start

2016-09-26

Marketing end

0000-00-00

Substance

ALBUTEROL SULFATE

Active strength

2 mg/5mL

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