NDC 68462-332 – Pramipexole dihydrochloride
Pramipexole Dihydrochloride .5 mg/1 · Tablet · Oral
Product NDC68462-332
Product details
- Brand name
- Pramipexole dihydrochloride
- Generic name
- Pramipexole dihydrochloride
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA090781
- Marketed since
- October 8, 2010
- Listing expires
- December 31, 2026
- Pharmacologic class
- Nonergot Dopamine Agonist
Active ingredients
- Pramipexole Dihydrochloride .5 mg/1
Uses, dosage, side effects and warnings for pramipexole dihydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 68462-332-05 | 500 TABLET in 1 BOTTLE (68462-332-05) | Oct 8, 2010 |
| 68462-332-11 | 10 BLISTER PACK in 1 CARTON (68462-332-11) / 10 TABLET in 1 BLISTER PACK | Oct 8, 2010 |
| 68462-332-90 | 90 TABLET in 1 BOTTLE (68462-332-90) | Oct 8, 2010 |
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