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Ipratropium Bromide - 0054-0046-41 - (Ipratropium Bromide)

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Drug Information of Ipratropium Bromide

Product NDC: 0054-0046
Proprietary Name: Ipratropium Bromide
Non Proprietary Name: Ipratropium Bromide
Active Ingredient(s): 42    ug/1 & nbsp;   Ipratropium Bromide
Administration Route(s): NASAL
Dosage Form(s): SPRAY
Coding System: National Drug Codes(NDC)

Labeler Information of Ipratropium Bromide

Product NDC: 0054-0046
Labeler Name: Roxane Laboratories, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076598
Marketing Category: ANDA
Start Marketing Date: 20031115

Package Information of Ipratropium Bromide

Package NDC: 0054-0046-41
Package Description: 1 BOTTLE, SPRAY in 1 CARTON (0054-0046-41) > 165 SPRAY in 1 BOTTLE, SPRAY

NDC Information of Ipratropium Bromide

NDC Code 0054-0046-41
Proprietary Name Ipratropium Bromide
Package Description 1 BOTTLE, SPRAY in 1 CARTON (0054-0046-41) > 165 SPRAY in 1 BOTTLE, SPRAY
Product NDC 0054-0046
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ipratropium Bromide
Dosage Form Name SPRAY
Route Name NASAL
Start Marketing Date 20031115
Marketing Category Name ANDA
Labeler Name Roxane Laboratories, Inc
Substance Name IPRATROPIUM BROMIDE
Strength Number 42
Strength Unit ug/1
Pharmaceutical Classes Anticholinergic [EPC],Cholinergic Antagonists [MoA]

Complete Information of Ipratropium Bromide


General Information