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Ipratropium Bromide and Albuterol Sulfate - 0781-7146-29 - (Ipratropium Bromide and Albuterol Sulfate)

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Drug Information of Ipratropium Bromide and Albuterol Sulfate

Product NDC: 0781-7146
Proprietary Name: Ipratropium Bromide and Albuterol Sulfate
Non Proprietary Name: Ipratropium Bromide and Albuterol Sulfate
Active Ingredient(s): 3; .5    mg/3mL; mg/3mL & nbsp;   Ipratropium Bromide and Albuterol Sulfate
Administration Route(s): RESPIRATORY (INHALATION)
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ipratropium Bromide and Albuterol Sulfate

Product NDC: 0781-7146
Labeler Name: Sandoz Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202496
Marketing Category: ANDA
Start Marketing Date: 20130520

Package Information of Ipratropium Bromide and Albuterol Sulfate

Package NDC: 0781-7146-29
Package Description: 12 POUCH in 1 CARTON (0781-7146-29) > 5 AMPULE in 1 POUCH (0781-7146-51) > 3 mL in 1 AMPULE

NDC Information of Ipratropium Bromide and Albuterol Sulfate

NDC Code 0781-7146-29
Proprietary Name Ipratropium Bromide and Albuterol Sulfate
Package Description 12 POUCH in 1 CARTON (0781-7146-29) > 5 AMPULE in 1 POUCH (0781-7146-51) > 3 mL in 1 AMPULE
Product NDC 0781-7146
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ipratropium Bromide and Albuterol Sulfate
Dosage Form Name SOLUTION
Route Name RESPIRATORY (INHALATION)
Start Marketing Date 20130520
Marketing Category Name ANDA
Labeler Name Sandoz Inc.
Substance Name ALBUTEROL SULFATE; IPRATROPIUM BROMIDE
Strength Number 3; .5
Strength Unit mg/3mL; mg/3mL
Pharmaceutical Classes Anticholinergic [EPC],Cholinergic Antagonists [MoA],Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]

Complete Information of Ipratropium Bromide and Albuterol Sulfate


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