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Ampicillin and Sulbactam - 0409-2988-15 - (AMPICILLIN and SULBACTAM)

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Drug Information of Ampicillin and Sulbactam

Product NDC: 0409-2988
Proprietary Name: Ampicillin and Sulbactam
Non Proprietary Name: AMPICILLIN and SULBACTAM
Active Ingredient(s): 1; .5    g/1; g/1 & nbsp;   AMPICILLIN and SULBACTAM
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ampicillin and Sulbactam

Product NDC: 0409-2988
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090375
Marketing Category: ANDA
Start Marketing Date: 20120319

Package Information of Ampicillin and Sulbactam

Package NDC: 0409-2988-15
Package Description: 10 VIAL in 1 CARTON (0409-2988-15) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

NDC Information of Ampicillin and Sulbactam

NDC Code 0409-2988-15
Proprietary Name Ampicillin and Sulbactam
Package Description 10 VIAL in 1 CARTON (0409-2988-15) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Product NDC 0409-2988
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name AMPICILLIN and SULBACTAM
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20120319
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name AMPICILLIN SODIUM; SULBACTAM SODIUM
Strength Number 1; .5
Strength Unit g/1; g/1
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient],beta Lactamase Inhibitors [MoA],beta Lactamase Inhibitor [EPC]

Complete Information of Ampicillin and Sulbactam


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