Ampicillin - 55150-111-10 - (Ampicillin Sodium)

Alphabetical Index


Drug Information of Ampicillin

Product NDC: 55150-111
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: 55150-111
Labeler Name: AuroMedics Pharma LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065499
Marketing Category: ANDA
Start Marketing Date: 20120201

Package Information of Ampicillin

Package NDC: 55150-111-10
Package Description: 10 VIAL in 1 BOX (55150-111-10) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

NDC Information of Ampicillin

NDC Code 55150-111-10
Proprietary Name Ampicillin
Package Description 10 VIAL in 1 BOX (55150-111-10) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Product NDC 55150-111
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 20120201
Marketing Category Name ANDA
Labeler Name AuroMedics Pharma LLC
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