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Nafcillin Sodium
Nafcillin Sodium - 0781-3128-92 - (Nafcillin Sodium)
Drug Information of Nafcillin Sodium
| Product NDC: | 0781-3128 |
| Proprietary Name: | Nafcillin Sodium |
| Non Proprietary Name: | Nafcillin Sodium |
| Active Ingredient(s): | 1 g/1 & nbsp; Nafcillin Sodium |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nafcillin Sodium
| Product NDC: | 0781-3128 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA062732 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050923 |
Package Information of Nafcillin Sodium
| Package NDC: | 0781-3128-92 |
| Package Description: | 10 VIAL, PATENT DELIVERY SYSTEM in 1 PACKAGE (0781-3128-92) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, PATENT DELIVERY SYSTEM (0781-3128-15) |
NDC Information of Nafcillin Sodium
| NDC Code | 0781-3128-92 |
| Proprietary Name | Nafcillin Sodium |
| Package Description | 10 VIAL, PATENT DELIVERY SYSTEM in 1 PACKAGE (0781-3128-92) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, PATENT DELIVERY SYSTEM (0781-3128-15) |
| Product NDC | 0781-3128 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Nafcillin Sodium |
| Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20050923 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | NAFCILLIN SODIUM |
| Strength Number | 1 |
| Strength Unit | g/1 |
| Pharmaceutical Classes | Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient] |
