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Ampicillin and Sulbactam - 55150-117-20 - (Ampicillin Sodium and Sulbactam Sodium)

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Drug Information of Ampicillin and Sulbactam

Product NDC: 55150-117
Proprietary Name: Ampicillin and Sulbactam
Non Proprietary Name: Ampicillin Sodium and Sulbactam Sodium
Active Ingredient(s): 2; 1    g/1; g/1 & nbsp;   Ampicillin Sodium and Sulbactam Sodium
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: 55150-117
Labeler Name: AuroMedics Pharma LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090349
Marketing Category: ANDA
Start Marketing Date: 20120210

Package Information of Ampicillin and Sulbactam

Package NDC: 55150-117-20
Package Description: 10 VIAL in 1 CARTON (55150-117-20) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

NDC Information of Ampicillin and Sulbactam

NDC Code 55150-117-20
Proprietary Name Ampicillin and Sulbactam
Package Description 10 VIAL in 1 CARTON (55150-117-20) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Product NDC 55150-117
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ampicillin Sodium and Sulbactam Sodium
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20120210
Marketing Category Name ANDA
Labeler Name AuroMedics Pharma LLC
Substance Name AMPICILLIN SODIUM; SULBACTAM SODIUM
Strength Number 2; 1
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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