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Ipratropium Bromide - 54868-5049-0 - (Ipratropium Bromide)

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Drug Information of Ipratropium Bromide

Product NDC: 54868-5049
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, METERED
Coding System: National Drug Codes(NDC)

Labeler Information of Ipratropium Bromide

Product NDC: 54868-5049
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076103
Marketing Category: ANDA
Start Marketing Date: 20040412

Package Information of Ipratropium Bromide

Package NDC: 54868-5049-0
Package Description: 1 BOTTLE, SPRAY in 1 CARTON (54868-5049-0) > 165 SPRAY, METERED in 1 BOTTLE, SPRAY

NDC Information of Ipratropium Bromide

NDC Code 54868-5049-0
Proprietary Name Ipratropium Bromide
Package Description 1 BOTTLE, SPRAY in 1 CARTON (54868-5049-0) > 165 SPRAY, METERED in 1 BOTTLE, SPRAY
Product NDC 54868-5049
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ipratropium Bromide
Dosage Form Name SPRAY, METERED
Route Name NASAL
Start Marketing Date 20040412
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name IPRATROPIUM BROMIDE
Strength Number 42
Strength Unit ug/1
Pharmaceutical Classes

Complete Information of Ipratropium Bromide


General Information