Flucytosine
Ancobon (flucytosine) is a small molecule pharmaceutical. Flucytosine was first approved as Ancobon on 1982-01-01. It is used to treat aids-related opportunistic infections, aspergillosis, candidiasis, chromoblastomycosis, and cryptococcal meningitis amongst others in the USA.
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Commercial
Trade Name
FDA
EMA
Ancobon (generic drugs available since 2011-06-28)
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Flucytosine
Tradename | Company | Number | Date | Products |
---|---|---|---|---|
ANCOBON | Bausch Health Companies | N-017001 RX | 1982-01-01 | 2 products, RLD, RS |
Labels
FDA
EMA
Brand Name | Status | Last Update |
---|---|---|
ancobon | New Drug Application | 2019-08-20 |
flucytosine | NDA authorized generic | 2023-03-16 |
Indications
FDA
EMA
Indication | Ontology | MeSH | ICD-10 |
---|---|---|---|
aids-related opportunistic infections | — | D017088 | — |
aspergillosis | EFO_0007157 | D001228 | B44 |
candidiasis | — | D002177 | B37 |
chromoblastomycosis | EFO_0007207 | D002862 | B43.9 |
cryptococcal meningitis | EFO_0007228 | D016919 | B45.1 |
mycoses | — | D009181 | B35-B49 |
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
D: Dermatologicals
— D01: Antifungals for dermatological use
— D01A: Antifungals for topical use
— D01AE: Other antifungals for topical use in atc
— D01AE21: Flucytosine
J: Antiinfectives for systemic use
— J02: Antimycotics for systemic use
— J02A: Antimycotics for systemic use
— J02AX: Other antimycotics for systemic use in atc
— J02AX01: Flucytosine
HCPCS
No data
Clinical
Clinical Trials
52 clinical trials
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Indications Phases 4
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Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Cholangiocarcinoma | D018281 | C22.1 | 3 | 7 | — | — | — | 9 | |
Stomach neoplasms | D013274 | EFO_0003897 | C16 | — | 8 | — | — | — | 8 |
Liver neoplasms | D008113 | EFO_1001513 | C22.0 | 2 | 2 | — | — | — | 4 |
Colonic neoplasms | D003110 | C18 | 2 | 3 | — | — | — | 4 | |
Rectal neoplasms | D012004 | 2 | 3 | — | — | — | 4 | ||
Esophageal neoplasms | D004938 | C15 | — | 3 | — | — | — | 3 | |
Adenocarcinoma | D000230 | — | 3 | — | — | — | 3 | ||
Bile duct neoplasms | D001650 | — | 1 | — | — | 1 | 2 | ||
Ovarian neoplasms | D010051 | EFO_0003893 | C56 | 1 | 1 | — | — | — | 2 |
Pancreatic neoplasms | D010190 | EFO_0003860 | C25 | — | 1 | — | — | — | 1 |
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Indications Phases 1
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Neoplasm metastasis | D009362 | EFO_0009708 | 2 | — | — | — | — | 2 | |
Nasopharyngeal neoplasms | D009303 | 1 | — | — | — | — | 1 | ||
Fallopian tube neoplasms | D005185 | 1 | — | — | — | — | 1 |
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name | FLUCYTOSINE |
INN | flucytosine |
Description | Flucytosine is an organofluorine compound that is cytosine that is substituted at position 5 by a fluorine. A prodrug for the antifungal 5-fluorouracil, it is used for the treatment of systemic fungal infections. It has a role as a prodrug. It is an organofluorine compound, a pyrimidone, an aminopyrimidine, a nucleoside analogue and a pyrimidine antifungal drug. It is functionally related to a cytosine. |
Classification | Small molecule |
Drug class | — |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | Nc1nc(=O)[nH]cc1F |
Identifiers
PDB | — |
CAS-ID | 2022-85-7 |
RxCUI | 4451 |
ChEMBL ID | CHEMBL1463 |
ChEBI ID | 5100 |
PubChem CID | 3366 |
DrugBank | DB01099 |
UNII ID | D83282DT06 (ChemIDplus, GSRS) |
Target
Agency Approved
No data
Alternate
No data
Variants
Clinical Variant
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Financial
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Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 6,045 documents
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Safety
Black-box Warning
Black-box warning for: Ancobon, Flucytosine
Adverse Events
Top Adverse Reactions
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71 adverse events reported
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