United States · FDA National Drug Code directory
DUTASTERIDE
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
- 84091-100_aff70ad7-652a-496f-b351-58c3ebd446e9
- Product NDC
- 84091-100
- Form
- CAPSULE
- Composition / generic term
- DUTASTERIDE
- Labeler
- Banyan Pharma LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20251231
- Source listing expiry
- 20271231
Source-listed ingredients
- DUTASTERIDE — .5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 90 CAPSULE in 1 BOTTLE (84091-100-90) · 84091-100-90
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 →