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Proventil HFA - 49999-907-67 - (Albuterol Sulfate)

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Drug Information of Proventil HFA

Product NDC: 49999-907
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: 49999-907
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020503
Marketing Category: NDA
Start Marketing Date: 20011001

Package Information of Proventil HFA

Package NDC: 49999-907-67
Package Description: 1 AEROSOL, METERED in 1 CARTON (49999-907-67)

NDC Information of Proventil HFA

NDC Code 49999-907-67
Proprietary Name Proventil HFA
Package Description 1 AEROSOL, METERED in 1 CARTON (49999-907-67)
Product NDC 49999-907
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Albuterol Sulfate
Dosage Form Name AEROSOL, METERED
Route Name RESPIRATORY (INHALATION)
Start Marketing Date 20011001
Marketing Category Name NDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
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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