Combivent - 54868-4225-0 - (ipratropium bromide and albuterol sulfate)

Alphabetical Index


Drug Information of Combivent

Product NDC: 54868-4225
Proprietary Name: Combivent
Non Proprietary Name: ipratropium bromide and albuterol sulfate
Active Ingredient(s): 103; 18    ug/1; ug/1 & nbsp;   ipratropium bromide and albuterol sulfate
Administration Route(s): RESPIRATORY (INHALATION)
Dosage Form(s): AEROSOL, METERED
Coding System: National Drug Codes(NDC)

Labeler Information of Combivent

Product NDC: 54868-4225
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020291
Marketing Category: NDA
Start Marketing Date: 20000918

Package Information of Combivent

Package NDC: 54868-4225-0
Package Description: 1 CANISTER in 1 CARTON (54868-4225-0) > 200 AEROSOL, METERED in 1 CANISTER

NDC Information of Combivent

NDC Code 54868-4225-0
Proprietary Name Combivent
Package Description 1 CANISTER in 1 CARTON (54868-4225-0) > 200 AEROSOL, METERED in 1 CANISTER
Product NDC 54868-4225
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ipratropium bromide and albuterol sulfate
Dosage Form Name AEROSOL, METERED
Route Name RESPIRATORY (INHALATION)
Start Marketing Date 20000918
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name ALBUTEROL SULFATE; IPRATROPIUM BROMIDE
Strength Number 103; 18
Strength Unit ug/1; ug/1
Pharmaceutical Classes Anticholinergic [EPC],Cholinergic Antagonists [MoA],Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]

Complete Information of Combivent


General Information