Oxacillin - 0781-3094-92 - (Oxacillin)

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Drug Information of Oxacillin

Product NDC: 0781-3094
Proprietary Name: Oxacillin
Non Proprietary Name: Oxacillin
Active Ingredient(s): 1    g/1 & nbsp;   Oxacillin
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Oxacillin

Product NDC: 0781-3094
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062737
Marketing Category: ANDA
Start Marketing Date: 19861223

Package Information of Oxacillin

Package NDC: 0781-3094-92
Package Description: 10 VIAL in 1 PACKAGE (0781-3094-92) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0781-3094-15)

NDC Information of Oxacillin

NDC Code 0781-3094-92
Proprietary Name Oxacillin
Package Description 10 VIAL in 1 PACKAGE (0781-3094-92) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0781-3094-15)
Product NDC 0781-3094
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxacillin
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19861223
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name OXACILLIN SODIUM
Strength Number 1
Strength Unit g/1
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient]

Complete Information of Oxacillin


General Information