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Nafcillin
Nafcillin - 63323-330-60 - (NAFCILLIN)
Drug Information of Nafcillin
| Product NDC: | 63323-330 |
| Proprietary Name: | Nafcillin |
| Non Proprietary Name: | NAFCILLIN |
| Active Ingredient(s): | 10 g/100mL & nbsp; NAFCILLIN |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nafcillin
| Product NDC: | 63323-330 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090005 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110427 |
Package Information of Nafcillin
| Package NDC: | 63323-330-60 |
| Package Description: | 1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (63323-330-60) > 100 mL in 1 VIAL, PHARMACY BULK PACKAGE |
NDC Information of Nafcillin
| NDC Code | 63323-330-60 |
| Proprietary Name | Nafcillin |
| Package Description | 1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (63323-330-60) > 100 mL in 1 VIAL, PHARMACY BULK PACKAGE |
| Product NDC | 63323-330 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | NAFCILLIN |
| Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20110427 |
| Marketing Category Name | ANDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | NAFCILLIN SODIUM |
| Strength Number | 10 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes | Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient] |
