Ampicillin - 55154-9384-5 - (ampicillin sodium)

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Drug Information of Ampicillin

Product NDC: 55154-9384
Proprietary Name: Ampicillin
Non Proprietary Name: ampicillin sodium
Active Ingredient(s): 2    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: 55154-9384
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062797
Marketing Category: ANDA
Start Marketing Date: 19930712

Package Information of Ampicillin

Package NDC: 55154-9384-5
Package Description: 5 VIAL in 1 BAG (55154-9384-5) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

NDC Information of Ampicillin

NDC Code 55154-9384-5
Proprietary Name Ampicillin
Package Description 5 VIAL in 1 BAG (55154-9384-5) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Product NDC 55154-9384
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 19930712
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name AMPICILLIN SODIUM
Strength Number 2
Strength Unit g/1
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient]

Complete Information of Ampicillin


General Information