United States · FDA National Drug Code directory
Nitisinone
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
- 70505-220_f74e0d5c-aaae-4751-a24d-4d141dfcae61
- Product NDC
- 70505-220
- Form
- CAPSULE
- Composition / generic term
- Nitisinone
- Labeler
- Analog Pharma
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230508
- Source listing expiry
- 20261231
Source-listed ingredients
- NITISINONE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, PLASTIC in 1 CARTON (70505-220-60) / 60 CAPSULE in 1 BOTTLE, PLASTIC · 70505-220-60
Source and coverage
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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.
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