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OXACILLIN
OXACILLIN - 0338-1015-41 - (OXACILLIN)
Drug Information of OXACILLIN
| Product NDC: | 0338-1015 |
| Proprietary Name: | OXACILLIN |
| Non Proprietary Name: | OXACILLIN |
| Active Ingredient(s): | 2 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: | 0338-1015 |
| 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: | 0338-1015-41 |
| Package Description: | 50 mL in 1 BAG (0338-1015-41) |
NDC Information of OXACILLIN
| NDC Code | 0338-1015-41 |
| Proprietary Name | OXACILLIN |
| Package Description | 50 mL in 1 BAG (0338-1015-41) |
| Product NDC | 0338-1015 |
| 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 | 2 |
| Strength Unit | g/50mL |
| Pharmaceutical Classes | Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient] |
