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AtroventHFA - 54868-5511-0 - (ipratropium bromide)

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Drug Information of AtroventHFA

Product NDC: 54868-5511
Proprietary Name: AtroventHFA
Non Proprietary Name: ipratropium bromide
Active Ingredient(s): 17    ug/1 & nbsp;   ipratropium bromide
Administration Route(s): RESPIRATORY (INHALATION)
Dosage Form(s): AEROSOL, METERED
Coding System: National Drug Codes(NDC)

Labeler Information of AtroventHFA

Product NDC: 54868-5511
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021527
Marketing Category: NDA
Start Marketing Date: 20060120

Package Information of AtroventHFA

Package NDC: 54868-5511-0
Package Description: 1 CANISTER in 1 CARTON (54868-5511-0) > 200 AEROSOL, METERED in 1 CANISTER

NDC Information of AtroventHFA

NDC Code 54868-5511-0
Proprietary Name AtroventHFA
Package Description 1 CANISTER in 1 CARTON (54868-5511-0) > 200 AEROSOL, METERED in 1 CANISTER
Product NDC 54868-5511
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ipratropium bromide
Dosage Form Name AEROSOL, METERED
Route Name RESPIRATORY (INHALATION)
Start Marketing Date 20060120
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name IPRATROPIUM BROMIDE
Strength Number 17
Strength Unit ug/1
Pharmaceutical Classes

Complete Information of AtroventHFA


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