Ampicillin - 10515-772-00 - (Ampicillin Sodium)

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Drug Information of Ampicillin

Product NDC: 10515-772
Proprietary Name: Ampicillin
Non Proprietary Name: Ampicillin Sodium
Active Ingredient(s): 1    g/1 & nbsp;   Ampicillin Sodium
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ampicillin

Product NDC: 10515-772
Labeler Name: GC Hanford Manufacturing Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062772
Marketing Category: ANDA
Start Marketing Date: 20080215

Package Information of Ampicillin

Package NDC: 10515-772-00
Package Description: 10 VIAL, GLASS in 1 TRAY (10515-772-00) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS

NDC Information of Ampicillin

NDC Code 10515-772-00
Proprietary Name Ampicillin
Package Description 10 VIAL, GLASS in 1 TRAY (10515-772-00) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS
Product NDC 10515-772
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ampicillin Sodium
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20080215
Marketing Category Name ANDA
Labeler Name GC Hanford Manufacturing Company
Substance Name AMPICILLIN SODIUM
Strength Number 1
Strength Unit g/1
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient]

Complete Information of Ampicillin


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