Ampicillin - 0781-9408-95 - (Ampicillin sodium)

Alphabetical Index


Drug Information of Ampicillin

Product NDC: 0781-9408
Proprietary Name: Ampicillin
Non Proprietary Name: Ampicillin sodium
Active Ingredient(s): 2    g/1 & 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: 0781-9408
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA061395
Marketing Category: ANDA
Start Marketing Date: 19710303

Package Information of Ampicillin

Package NDC: 0781-9408-95
Package Description: 10 VIAL, GLASS in 1 PACKAGE (0781-9408-95) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS (0781-9408-80)

NDC Information of Ampicillin

NDC Code 0781-9408-95
Proprietary Name Ampicillin
Package Description 10 VIAL, GLASS in 1 PACKAGE (0781-9408-95) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS (0781-9408-80)
Product NDC 0781-9408
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ampicillin sodium
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19710303
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name AMPICILLIN SODIUM
Strength Number 2
Strength Unit g/1
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient]

Complete Information of Ampicillin


General Information