Ampicillin - 52584-389-10 - (Ampicillin Sodium)

Alphabetical Index


Drug Information of Ampicillin

Product NDC: 52584-389
Proprietary Name: Ampicillin
Non Proprietary Name: Ampicillin Sodium
Active Ingredient(s): 1    g/g & nbsp;   Ampicillin Sodium
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ampicillin

Product NDC: 52584-389
Labeler Name: General Injectables & Vaccines, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062719
Marketing Category: ANDA
Start Marketing Date: 20100401

Package Information of Ampicillin

Package NDC: 52584-389-10
Package Description: 1 VIAL in 1 BAG (52584-389-10) > 1 g in 1 VIAL

NDC Information of Ampicillin

NDC Code 52584-389-10
Proprietary Name Ampicillin
Package Description 1 VIAL in 1 BAG (52584-389-10) > 1 g in 1 VIAL
Product NDC 52584-389
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ampicillin Sodium
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20100401
Marketing Category Name ANDA
Labeler Name General Injectables & Vaccines, Inc
Substance Name AMPICILLIN SODIUM
Strength Number 1
Strength Unit g/g
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient]

Complete Information of Ampicillin


General Information