Home
>
National Drug Code (NDC)
>
Flucytosine
Flucytosine - 68682-356-10 - (Flucytosine)
Drug Information of Flucytosine
| Product NDC: | 68682-356 |
| 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: | 68682-356 |
| Labeler Name: | Oceanside Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA017001 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20120117 |
Package Information of Flucytosine
| Package NDC: | 68682-356-10 |
| Package Description: | 100 CAPSULE in 1 BOTTLE (68682-356-10) |
NDC Information of Flucytosine
| NDC Code | 68682-356-10 |
| Proprietary Name | Flucytosine |
| Package Description | 100 CAPSULE in 1 BOTTLE (68682-356-10) |
| Product NDC | 68682-356 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Flucytosine |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20120117 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Oceanside Pharmaceuticals |
| Substance Name | FLUCYTOSINE |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Nucleoside Analog [Chemical/Ingredient],Nucleoside Analog Antifungal [EPC] |
