Albuterol Sulfate

Product NDC

68788-0134

11-digit product format

687880134

Labeler code

68788

Product ID

68788-0134_04d577a3-73ed-40bf-a527-45861bf5b2f1

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Albuterol Sulfate

Dosage form

SOLUTION

Route

RESPIRATORY (INHALATION)

Labeler

Preferred Pharmaceuticals, Inc

Application

ANDA074880

Marketing category

ANDA

Marketing start

1997-09-17

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

2019-12-31

Current FDA listing

Historical FDA.report record