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Flucytosine
Flucytosine - 64980-180-01 - (Flucytosine)
Drug Information of Flucytosine
| Product NDC: | 64980-180 |
| Proprietary Name: | Flucytosine |
| 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 Flucytosine
| Product NDC: | 64980-180 |
| Labeler Name: | Rising Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA201566 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110715 |
Package Information of Flucytosine
| Package NDC: | 64980-180-01 |
| Package Description: | 100 CAPSULE in 1 BOTTLE (64980-180-01) |
NDC Information of Flucytosine
| NDC Code | 64980-180-01 |
| Proprietary Name | Flucytosine |
| Package Description | 100 CAPSULE in 1 BOTTLE (64980-180-01) |
| Product NDC | 64980-180 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Flucytosine |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20110715 |
| Marketing Category Name | ANDA |
| Labeler Name | Rising Pharmaceuticals, Inc. |
| Substance Name | FLUCYTOSINE |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Nucleoside Analog [Chemical/Ingredient],Nucleoside Analog Antifungal [EPC] |
