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
- 33342-209_4bae794e-6b1f-4630-9d00-a4524fffa0b9
- Product NDC
- 33342-209
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Pramipexole Dihydrochloride
- Labeler
- Macleods Pharmaceuticals Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200824
- Source listing expiry
- 20261231
Source-listed ingredients
- PRAMIPEXOLE DIHYDROCHLORIDE — .75 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-209-07) · 33342-209-07
- 10 BLISTER PACK in 1 CARTON (33342-209-12) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK · 33342-209-12
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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