OXACILLIN - 0338-1013-41 - (OXACILLIN)

Alphabetical Index


Drug Information of OXACILLIN

Product NDC: 0338-1013
Proprietary Name: OXACILLIN
Non Proprietary Name: OXACILLIN
Active Ingredient(s): 1    g/50mL & nbsp;   OXACILLIN
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of OXACILLIN

Product NDC: 0338-1013
Labeler Name: Baxter Healthcare Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050640
Marketing Category: NDA
Start Marketing Date: 19891026

Package Information of OXACILLIN

Package NDC: 0338-1013-41
Package Description: 50 mL in 1 BAG (0338-1013-41)

NDC Information of OXACILLIN

NDC Code 0338-1013-41
Proprietary Name OXACILLIN
Package Description 50 mL in 1 BAG (0338-1013-41)
Product NDC 0338-1013
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name OXACILLIN
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19891026
Marketing Category Name NDA
Labeler Name Baxter Healthcare Corporation
Substance Name OXACILLIN SODIUM
Strength Number 1
Strength Unit g/50mL
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient]

Complete Information of OXACILLIN


General Information