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Ipratropium Bromide - 0781-7157-29 - (Ipratropium Bromide)

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Drug Information of Ipratropium Bromide

Product NDC: 0781-7157
Proprietary Name: Ipratropium Bromide
Non Proprietary Name: Ipratropium Bromide
Active Ingredient(s): .5    mg/2.5mL & nbsp;   Ipratropium Bromide
Administration Route(s): RESPIRATORY (INHALATION)
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ipratropium Bromide

Product NDC: 0781-7157
Labeler Name: Sandoz Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075693
Marketing Category: ANDA
Start Marketing Date: 20110901

Package Information of Ipratropium Bromide

Package NDC: 0781-7157-29
Package Description: 2 POUCH in 1 CARTON (0781-7157-29) > 30 AMPULE in 1 POUCH > 2.5 mL in 1 AMPULE

NDC Information of Ipratropium Bromide

NDC Code 0781-7157-29
Proprietary Name Ipratropium Bromide
Package Description 2 POUCH in 1 CARTON (0781-7157-29) > 30 AMPULE in 1 POUCH > 2.5 mL in 1 AMPULE
Product NDC 0781-7157
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ipratropium Bromide
Dosage Form Name SOLUTION
Route Name RESPIRATORY (INHALATION)
Start Marketing Date 20110901
Marketing Category Name ANDA
Labeler Name Sandoz Inc.
Substance Name IPRATROPIUM BROMIDE
Strength Number .5
Strength Unit mg/2.5mL
Pharmaceutical Classes Anticholinergic [EPC],Cholinergic Antagonists [MoA]

Complete Information of Ipratropium Bromide


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