Ampicillin - 55154-9379-5 - (ampicillin sodium)

Alphabetical Index


Drug Information of Ampicillin

Product NDC: 55154-9379
Proprietary Name: Ampicillin
Non Proprietary Name: ampicillin sodium
Active Ingredient(s): 250    mg/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: 55154-9379
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062719
Marketing Category: ANDA
Start Marketing Date: 19870512

Package Information of Ampicillin

Package NDC: 55154-9379-5
Package Description: 5 VIAL in 1 BAG (55154-9379-5) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

NDC Information of Ampicillin

NDC Code 55154-9379-5
Proprietary Name Ampicillin
Package Description 5 VIAL in 1 BAG (55154-9379-5) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Product NDC 55154-9379
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 19870512
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name AMPICILLIN SODIUM
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient]

Complete Information of Ampicillin


General Information