Ampicillin - 0781-3407-95 - (Ampicillin sodium)

Alphabetical Index


Drug Information of Ampicillin

Product NDC: 0781-3407
Proprietary Name: Ampicillin
Non Proprietary Name: Ampicillin sodium
Active Ingredient(s): 500    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: 0781-3407
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: 0781-3407-95
Package Description: 10 VIAL, GLASS in 1 PACKAGE (0781-3407-95) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS (0781-3407-78)

NDC Information of Ampicillin

NDC Code 0781-3407-95
Proprietary Name Ampicillin
Package Description 10 VIAL, GLASS in 1 PACKAGE (0781-3407-95) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS (0781-3407-78)
Product NDC 0781-3407
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 19710303
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name AMPICILLIN SODIUM
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient]

Complete Information of Ampicillin


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