AMPICILLIN - 52584-135-10 - (ampicillin sodium)

Alphabetical Index


Drug Information of AMPICILLIN

Product NDC: 52584-135
Proprietary Name: AMPICILLIN
Non Proprietary Name: ampicillin sodium
Active Ingredient(s): 500    mg/500mg & 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: 52584-135
Labeler Name: General Injectables & Vaccines, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA063146
Marketing Category: ANDA
Start Marketing Date: 20130313

Package Information of AMPICILLIN

Package NDC: 52584-135-10
Package Description: 1 VIAL in 1 BAG (52584-135-10) > 500 mg in 1 VIAL

NDC Information of AMPICILLIN

NDC Code 52584-135-10
Proprietary Name AMPICILLIN
Package Description 1 VIAL in 1 BAG (52584-135-10) > 500 mg in 1 VIAL
Product NDC 52584-135
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 20130313
Marketing Category Name ANDA
Labeler Name General Injectables & Vaccines, Inc
Substance Name AMPICILLIN SODIUM
Strength Number 500
Strength Unit mg/500mg
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient]

Complete Information of AMPICILLIN


General Information