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ANCOBON
ANCOBON - 0187-3555-10 - (Flucytosine)
Drug Information of ANCOBON
| Product NDC: | 0187-3555 |
| Proprietary Name: | ANCOBON |
| Non Proprietary Name: | Flucytosine |
| Active Ingredient(s): | 500 mg/1 & nbsp; Flucytosine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ANCOBON
| Product NDC: | 0187-3555 |
| Labeler Name: | Valeant Pharmaceuticals North America LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA017001 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19711126 |
Package Information of ANCOBON
| Package NDC: | 0187-3555-10 |
| Package Description: | 100 CAPSULE in 1 BOTTLE (0187-3555-10) |
NDC Information of ANCOBON
| NDC Code | 0187-3555-10 |
| Proprietary Name | ANCOBON |
| Package Description | 100 CAPSULE in 1 BOTTLE (0187-3555-10) |
| Product NDC | 0187-3555 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Flucytosine |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19711126 |
| Marketing Category Name | NDA |
| Labeler Name | Valeant Pharmaceuticals North America LLC |
| Substance Name | FLUCYTOSINE |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Nucleoside Analog [Chemical/Ingredient],Nucleoside Analog Antifungal [EPC] |
