Ampicillin - 36000-072-10 - (Ampicillin sodium)

Alphabetical Index


Drug Information of Ampicillin

Product NDC: 36000-072
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: 36000-072
Labeler Name: Claris Lifesciences, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090354
Marketing Category: ANDA
Start Marketing Date: 20100425

Package Information of Ampicillin

Package NDC: 36000-072-10
Package Description: 10 VIAL in 1 CARTON (36000-072-10) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

NDC Information of Ampicillin

NDC Code 36000-072-10
Proprietary Name Ampicillin
Package Description 10 VIAL in 1 CARTON (36000-072-10) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Product NDC 36000-072
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 20100425
Marketing Category Name ANDA
Labeler Name Claris Lifesciences, Inc.
Substance Name AMPICILLIN SODIUM
Strength Number 1
Strength Unit g/1
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient]

Complete Information of Ampicillin


General Information