United States · FDA National Drug Code directory
ropinirole hydrochloride
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
- 71335-0587_d88b1f49-8ea3-43fa-ae34-0cb10ca3a562
- Product NDC
- 71335-0587
- Form
- TABLET, FILM COATED
- Composition / generic term
- ropinirole hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20110920
- Source listing expiry
- 20261231
Source-listed ingredients
- ROPINIROLE HYDROCHLORIDE — .25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-0587-1) · 71335-0587-1
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-0587-2) · 71335-0587-2
- 28 TABLET, FILM COATED in 1 BOTTLE (71335-0587-3) · 71335-0587-3
- 100 TABLET, FILM COATED in 1 BOTTLE (71335-0587-4) · 71335-0587-4
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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