United States · FDA National Drug Code directory
Pramipexole Dihydrochloride
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
- 63629-5013_067d8e1a-6550-4be0-8321-3918949ff552
- Product NDC
- 63629-5013
- Form
- TABLET
- Composition / generic term
- Pramipexole Dihydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20101008
- Source listing expiry
- 20271231
Source-listed ingredients
- PRAMIPEXOLE DIHYDROCHLORIDE — .25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 90 TABLET in 1 BOTTLE (63629-5013-1) · 63629-5013-1
- 30 TABLET in 1 BOTTLE (63629-5013-2) · 63629-5013-2
- 60 TABLET in 1 BOTTLE (63629-5013-3) · 63629-5013-3
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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