United States · FDA National Drug Code directory
PRAMIPEXOLE
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
- 31722-911_540a17f8-b64d-41e1-a96b-d55bc8c48f3d
- Product NDC
- 31722-911
- Form
- TABLET
- Composition / generic term
- PRAMIPEXOLE
- Labeler
- Camber Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150801
- Source listing expiry
- 20261231
Source-listed ingredients
- PRAMIPEXOLE DIHYDROCHLORIDE — 1.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 500 TABLET in 1 BOTTLE (31722-911-05) · 31722-911-05
- 1000 TABLET in 1 BOTTLE (31722-911-10) · 31722-911-10
- 90 TABLET in 1 BOTTLE (31722-911-90) · 31722-911-90
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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