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Ipratropium Bromide - 0378-6989-62 - (ipratropium bromide)

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Drug Information of Ipratropium Bromide

Product NDC: 0378-6989
Proprietary Name: Ipratropium Bromide
Non Proprietary Name: ipratropium bromide
Active Ingredient(s): 500    ug/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: 0378-6989
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075693
Marketing Category: ANDA
Start Marketing Date: 20101109

Package Information of Ipratropium Bromide

Package NDC: 0378-6989-62
Package Description: 25 POUCH in 1 CARTON (0378-6989-62) > 1 VIAL in 1 POUCH > 2.5 mL in 1 VIAL

NDC Information of Ipratropium Bromide

NDC Code 0378-6989-62
Proprietary Name Ipratropium Bromide
Package Description 25 POUCH in 1 CARTON (0378-6989-62) > 1 VIAL in 1 POUCH > 2.5 mL in 1 VIAL
Product NDC 0378-6989
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ipratropium bromide
Dosage Form Name SOLUTION
Route Name RESPIRATORY (INHALATION)
Start Marketing Date 20101109
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name IPRATROPIUM BROMIDE
Strength Number 500
Strength Unit ug/2.5mL
Pharmaceutical Classes Anticholinergic [EPC],Cholinergic Antagonists [MoA]

Complete Information of Ipratropium Bromide


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