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Ampicillin and Sulbactam - 25021-142-20 - (ampicillin and sulbactam)

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Drug Information of Ampicillin and Sulbactam

Product NDC: 25021-142
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: 25021-142
Labeler Name: Sagent Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065406
Marketing Category: ANDA
Start Marketing Date: 20100630

Package Information of Ampicillin and Sulbactam

Package NDC: 25021-142-20
Package Description: 10 INJECTION, POWDER, FOR SOLUTION in 1 CARTON (25021-142-20)

NDC Information of Ampicillin and Sulbactam

NDC Code 25021-142-20
Proprietary Name Ampicillin and Sulbactam
Package Description 10 INJECTION, POWDER, FOR SOLUTION in 1 CARTON (25021-142-20)
Product NDC 25021-142
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 20100630
Marketing Category Name ANDA
Labeler Name Sagent Pharmaceuticals, 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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