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Ampicillin and Sulbactam - 0409-2689-11 - (Ampicillin sodium and Sulbactam sodium)

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Drug Information of Ampicillin and Sulbactam

Product NDC: 0409-2689
Proprietary Name: Ampicillin and Sulbactam
Non Proprietary Name: Ampicillin sodium and Sulbactam sodium
Active Ingredient(s): 1; .5    g/1; g/1 & nbsp;   Ampicillin sodium and Sulbactam sodium
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ampicillin and Sulbactam

Product NDC: 0409-2689
Labeler Name: Hospira, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065241
Marketing Category: ANDA
Start Marketing Date: 20060725

Package Information of Ampicillin and Sulbactam

Package NDC: 0409-2689-11
Package Description: 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0409-2689-11)

NDC Information of Ampicillin and Sulbactam

NDC Code 0409-2689-11
Proprietary Name Ampicillin and Sulbactam
Package Description 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0409-2689-11)
Product NDC 0409-2689
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ampicillin sodium and Sulbactam sodium
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20060725
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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