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
- 68462-332_75644134-fcad-4dde-8a22-453d18472002
- Product NDC
- 68462-332
- Form
- TABLET
- Composition / generic term
- Pramipexole dihydrochloride
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20101008
- Source listing expiry
- 20261231
Source-listed ingredients
- PRAMIPEXOLE DIHYDROCHLORIDE — .5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 500 TABLET in 1 BOTTLE (68462-332-05) · 68462-332-05
- 10 BLISTER PACK in 1 CARTON (68462-332-11) / 10 TABLET in 1 BLISTER PACK · 68462-332-11
- 90 TABLET in 1 BOTTLE (68462-332-90) · 68462-332-90
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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