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