flucytosine
Generic: flucytosine
Labeler: major pharmaceuticalsDrug Facts
Product Profile
Brand Name
flucytosine
Generic Name
flucytosine
Labeler
major pharmaceuticals
Dosage Form
CAPSULE
Routes
Active Ingredients
flucytosine 250 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0904-6834
Product ID
0904-6834_f6d603f8-d4ee-4541-928a-eb81b26bd4db
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA204652
Listing Expiration
2027-12-31
Marketing Start
2017-07-07
Pharmacologic Class
Established (EPC)
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
09046834
Hyphenated Format
0904-6834
Supplemental Identifiers
RxCUI
UNII
NUI
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
flucytosine (source: ndc)
Generic Name
flucytosine (source: ndc)
Application Number
ANDA204652 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/1
Packaging
- 30 BLISTER PACK in 1 CARTON (0904-6834-07) / 1 CAPSULE in 1 BLISTER PACK
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f6d603f8-d4ee-4541-928a-eb81b26bd4db", "openfda": {"nui": ["N0000175459", "N0000175467"], "unii": ["D83282DT06"], "rxcui": ["197702", "197703"], "spl_set_id": ["01d874f9-e073-4092-94ad-da361551d4bf"], "pharm_class_epc": ["Nucleoside Analog Antifungal [EPC]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (0904-6834-07) / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "0904-6834-07", "marketing_start_date": "20170707"}], "brand_name": "Flucytosine", "product_id": "0904-6834_f6d603f8-d4ee-4541-928a-eb81b26bd4db", "dosage_form": "CAPSULE", "pharm_class": ["Nucleoside Analog Antifungal [EPC]", "Nucleoside Analog [EXT]"], "product_ndc": "0904-6834", "generic_name": "Flucytosine", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Flucytosine", "active_ingredients": [{"name": "FLUCYTOSINE", "strength": "250 mg/1"}], "application_number": "ANDA204652", "marketing_category": "ANDA", "marketing_start_date": "20170707", "listing_expiration_date": "20271231"}