Ampicillin - 44567-102-10 - (Ampicillin)

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Drug Information of Ampicillin

Product NDC: 44567-102
Proprietary Name: Ampicillin
Non Proprietary Name: Ampicillin
Active Ingredient(s): 1    g/1 & nbsp;   Ampicillin
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ampicillin

Product NDC: 44567-102
Labeler Name: WG Critical Care, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062772
Marketing Category: ANDA
Start Marketing Date: 20120510

Package Information of Ampicillin

Package NDC: 44567-102-10
Package Description: 10 VIAL in 1 TRAY (44567-102-10) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

NDC Information of Ampicillin

NDC Code 44567-102-10
Proprietary Name Ampicillin
Package Description 10 VIAL in 1 TRAY (44567-102-10) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Product NDC 44567-102
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ampicillin
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20120510
Marketing Category Name ANDA
Labeler Name WG Critical Care, LLC
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