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
- 64380-747_411af03f-06f1-4f2c-9f51-cacfef78233b
- Product NDC
- 64380-747
- Form
- TABLET
- Composition / generic term
- pramipexole dihydrochloride
- Labeler
- Strides Pharma Science Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210215
- Source listing expiry
- 20271231
Source-listed ingredients
- PRAMIPEXOLE DIHYDROCHLORIDE — .25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 BLISTER PACK in 1 CARTON (64380-747-01) / 10 TABLET in 1 BLISTER PACK · 64380-747-01
- 90 TABLET in 1 BOTTLE (64380-747-05) · 64380-747-05
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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