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
- 65862-604_1e01cf5f-29b7-40ce-8c46-40f8dc65ce3e
- Product NDC
- 65862-604
- Form
- TABLET
- Composition / generic term
- Pramipexole Dihydrochloride
- Labeler
- Aurobindo Pharma Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20121026
- Source listing expiry
- 20261231
Source-listed ingredients
- PRAMIPEXOLE DIHYDROCHLORIDE — .125 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 BLISTER PACK in 1 CARTON (65862-604-78) / 10 TABLET in 1 BLISTER PACK (65862-604-10) · 65862-604-78
- 90 TABLET in 1 BOTTLE (65862-604-90) · 65862-604-90
- 1000 TABLET in 1 BOTTLE (65862-604-99) · 65862-604-99
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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