Ipratropium Bromide and Albuterol Sulfate

Product NDC

0781-7146

11-digit product format

007817146

Labeler code

0781

Product ID

0781-7146_305bb6c8-61ad-41db-8086-d60792c8ea68

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ipratropium Bromide and Albuterol Sulfate

Dosage form

SOLUTION

Route

RESPIRATORY (INHALATION)

Labeler

Sandoz Inc.

Application

ANDA202496

Marketing category

ANDA

Marketing start

2013-05-20

Marketing end

0000-00-00

Substance

IPRATROPIUM BROMIDE; ALBUTEROL SULFATE

Active strength

1 mg/3mL; mg/3mL

Pharmacologic classes

Anticholinergic [EPC],Cholinergic Antagonists [MoA],Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record