Albuterol

Product NDC

69339-126

11-digit product format

693390126

Labeler code

69339

Product ID

69339-126_935a4e25-e6b1-4b04-e053-2a95a90ae5d6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

albuterol sulfate

Dosage form

TABLET

Route

ORAL

Labeler

Dash Pharmaceutical LLC

Application

ANDA210948

Marketing category

ANDA

Marketing start

2019-03-15

Marketing end

0000-00-00

Substance

ALBUTEROL SULFATE

Active strength

2 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