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Ampicillin and Sulbactam - 63323-369-20 - (ampicillin sodium and sulbactam sodium)

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Drug Information of Ampicillin and Sulbactam

Product NDC: 63323-369
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: 63323-369
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065222
Marketing Category: ANDA
Start Marketing Date: 20051129

Package Information of Ampicillin and Sulbactam

Package NDC: 63323-369-20
Package Description: 10 VIAL in 1 CARTON (63323-369-20) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

NDC Information of Ampicillin and Sulbactam

NDC Code 63323-369-20
Proprietary Name Ampicillin and Sulbactam
Package Description 10 VIAL in 1 CARTON (63323-369-20) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Product NDC 63323-369
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 20051129
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, 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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