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Proventil HFA - 54868-6051-0 - (albuterol sulfate)

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Drug Information of Proventil HFA

Product NDC: 54868-6051
Proprietary Name: Proventil HFA
Non Proprietary Name: albuterol sulfate
Active Ingredient(s): 108    ug/1 & nbsp;   albuterol sulfate
Administration Route(s): RESPIRATORY (INHALATION)
Dosage Form(s): AEROSOL, METERED
Coding System: National Drug Codes(NDC)

Labeler Information of Proventil HFA

Product NDC: 54868-6051
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020503
Marketing Category: NDA
Start Marketing Date: 20090717

Package Information of Proventil HFA

Package NDC: 54868-6051-0
Package Description: 200 AEROSOL, METERED in 1 INHALER (54868-6051-0)

NDC Information of Proventil HFA

NDC Code 54868-6051-0
Proprietary Name Proventil HFA
Package Description 200 AEROSOL, METERED in 1 INHALER (54868-6051-0)
Product NDC 54868-6051
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name albuterol sulfate
Dosage Form Name AEROSOL, METERED
Route Name RESPIRATORY (INHALATION)
Start Marketing Date 20090717
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name ALBUTEROL SULFATE
Strength Number 108
Strength Unit ug/1
Pharmaceutical Classes Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]

Complete Information of Proventil HFA


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