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Proventil HFA - 0085-1132-01 - (Albuterol Sulfate)

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Drug Information of Proventil HFA

Product NDC: 0085-1132
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: 0085-1132
Labeler Name: Merck Sharp & Dohme Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020503
Marketing Category: NDA
Start Marketing Date: 20011001

Package Information of Proventil HFA

Package NDC: 0085-1132-01
Package Description: 1 CANISTER in 1 CARTON (0085-1132-01) > 200 AEROSOL, METERED in 1 CANISTER

NDC Information of Proventil HFA

NDC Code 0085-1132-01
Proprietary Name Proventil HFA
Package Description 1 CANISTER in 1 CARTON (0085-1132-01) > 200 AEROSOL, METERED in 1 CANISTER
Product NDC 0085-1132
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 Merck Sharp & Dohme Corp.
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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