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Nafcillin
Nafcillin - 36000-175-10 - (Nafcillin)
Drug Information of Nafcillin
| Product NDC: | 36000-175 |
| Proprietary Name: | Nafcillin |
| Non Proprietary Name: | Nafcillin |
| Active Ingredient(s): | 1 g/1 & nbsp; Nafcillin |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nafcillin
| Product NDC: | 36000-175 |
| Labeler Name: | Claris Lifesciences, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090560 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120201 |
Package Information of Nafcillin
| Package NDC: | 36000-175-10 |
| Package Description: | 10 VIAL in 1 PACKAGE (36000-175-10) > 1 INJECTION in 1 VIAL (36000-175-01) |
NDC Information of Nafcillin
| NDC Code | 36000-175-10 |
| Proprietary Name | Nafcillin |
| Package Description | 10 VIAL in 1 PACKAGE (36000-175-10) > 1 INJECTION in 1 VIAL (36000-175-01) |
| Product NDC | 36000-175 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Nafcillin |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20120201 |
| Marketing Category Name | ANDA |
| Labeler Name | Claris Lifesciences, Inc. |
| Substance Name | NAFCILLIN SODIUM |
| Strength Number | 1 |
| Strength Unit | g/1 |
| Pharmaceutical Classes | Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient] |
