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Oxacillin
Oxacillin - 0781-9109-95 - (Oxacillin)
Drug Information of Oxacillin
| Product NDC: | 0781-9109 |
| Proprietary Name: | Oxacillin |
| Non Proprietary Name: | Oxacillin |
| Active Ingredient(s): | 1 g/1 & nbsp; Oxacillin |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Oxacillin
| Product NDC: | 0781-9109 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA061490 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19760106 |
Package Information of Oxacillin
| Package NDC: | 0781-9109-95 |
| Package Description: | 10 VIAL in 1 PACKAGE (0781-9109-95) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0781-9109-85) |
NDC Information of Oxacillin
| NDC Code | 0781-9109-95 |
| Proprietary Name | Oxacillin |
| Package Description | 10 VIAL in 1 PACKAGE (0781-9109-95) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0781-9109-85) |
| Product NDC | 0781-9109 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Oxacillin |
| Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 19760106 |
| 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] |
