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Albuterol Sulfate - 54868-2887-0 - (Albuterol Sulfate)

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Drug Information of Albuterol Sulfate

Product NDC: 54868-2887
Proprietary Name: Albuterol Sulfate
Non Proprietary Name: Albuterol Sulfate
Active Ingredient(s): 2    mg/5mL & nbsp;   Albuterol Sulfate
Administration Route(s): ORAL
Dosage Form(s): SYRUP
Coding System: National Drug Codes(NDC)

Labeler Information of Albuterol Sulfate

Product NDC: 54868-2887
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074749
Marketing Category: ANDA
Start Marketing Date: 19941013

Package Information of Albuterol Sulfate

Package NDC: 54868-2887-0
Package Description: 473 mL in 1 BOTTLE (54868-2887-0)

NDC Information of Albuterol Sulfate

NDC Code 54868-2887-0
Proprietary Name Albuterol Sulfate
Package Description 473 mL in 1 BOTTLE (54868-2887-0)
Product NDC 54868-2887
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Albuterol Sulfate
Dosage Form Name SYRUP
Route Name ORAL
Start Marketing Date 19941013
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name ALBUTEROL SULFATE
Strength Number 2
Strength Unit mg/5mL
Pharmaceutical Classes Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]

Complete Information of Albuterol Sulfate


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