NDC 16714-917 – Pramipexole Dihydrochloride
Pramipexole Dihydrochloride .75 mg/1 · Tablet, Extended Release · Oral
Product NDC16714-917
Product details
- Brand name
- Pramipexole Dihydrochloride
- Generic name
- Pramipexole Dihydrochloride
- Labeler
- NorthStar RxLLC
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA206156
- Marketed since
- March 6, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- Nonergot Dopamine Agonist
Active ingredients
- Pramipexole Dihydrochloride .75 mg/1
Uses, dosage, side effects and warnings for pramipexole dihydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 16714-917-01 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-917-01) | Mar 6, 2019 |
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