FLUCYTOSINE
NDC 59651-332, FLUCYTOSINE, capsule, from Aurobindo Pharma Limited.
- Product NDC
- 59651-332
- Status
- Listed
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- CAPSULE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA213665
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/59651-332 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FLUCYTOSINE500 mg/1
Pharmacologic classes
Nucleoside Analog Antifungal [EPC]; Nucleoside Analog [EXT]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 59651-332-01 | 59651033201 | 100 CAPSULE in 1 BOTTLE (59651-332-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/8b55832c-6771-4f5b-9aef-f88a1d22795e
Use it
Look up 59651-332 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/59651-332 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 59651-332. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.