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NOXAFIL
NOXAFIL - 0085-1328-01 - (posaconazole)
Drug Information of NOXAFIL
| Product NDC: | 0085-1328 |
| Proprietary Name: | NOXAFIL |
| Non Proprietary Name: | posaconazole |
| Active Ingredient(s): | 40 mg/mL & nbsp; posaconazole |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NOXAFIL
| Product NDC: | 0085-1328 |
| Labeler Name: | Merck Sharp & Dohme Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022003 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20060915 |
Package Information of NOXAFIL
| Package NDC: | 0085-1328-01 |
| Package Description: | 1 BOTTLE, GLASS in 1 CARTON (0085-1328-01) > 105 mL in 1 BOTTLE, GLASS |
NDC Information of NOXAFIL
| NDC Code | 0085-1328-01 |
| Proprietary Name | NOXAFIL |
| Package Description | 1 BOTTLE, GLASS in 1 CARTON (0085-1328-01) > 105 mL in 1 BOTTLE, GLASS |
| Product NDC | 0085-1328 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | posaconazole |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20060915 |
| Marketing Category Name | NDA |
| Labeler Name | Merck Sharp & Dohme Corp. |
| Substance Name | POSACONAZOLE |
| Strength Number | 40 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |
