United States · FDA National Drug Code directory
Flucytosine
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 42385-983_2aaf23f5-9b8f-4c5a-8c90-5c83765ad889
- Product NDC
- 42385-983
- Form
- CAPSULE
- Composition / generic term
- Flucytosine
- Labeler
- Laurus Labs Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250724
- Source listing expiry
- 20261231
Source-listed ingredients
- FLUCYTOSINE — 250 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE in 1 BOTTLE (42385-983-01) · 42385-983-01
- 10 BLISTER PACK in 1 CARTON (42385-983-27) / 10 CAPSULE in 1 BLISTER PACK · 42385-983-27
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →