NDC 33342-033 – Pramipexole dihydrochloride
Pramipexole Dihydrochloride .5 mg/1 · Tablet · Oral
Product NDC33342-033
Product details
- Brand name
- Pramipexole dihydrochloride
- Generic name
- Pramipexole dihydrochloride
- Labeler
- Macleods Pharmaceuticals Limited
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA202164
- Marketed since
- September 21, 2012
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 33342-033-06 | 30 BLISTER PACK in 1 CARTON (33342-033-06) / 1 TABLET in 1 BLISTER PACK | Sep 21, 2012 |
| 33342-033-10 | 90 TABLET in 1 BOTTLE (33342-033-10) | Sep 21, 2012 |
| 33342-033-12 | 100 BLISTER PACK in 1 CARTON (33342-033-12) / 1 TABLET in 1 BLISTER PACK | Sep 21, 2012 |
| 33342-033-15 | 500 TABLET in 1 BOTTLE (33342-033-15) | Sep 21, 2012 |
Recalls mentioning this NDC
- D-1851-2019 Sep 18, 2019 · Class III
Subpotent Drug: Out of specification result during stability study in Pramipexole Dihydrochloride Tablets 0.125 mg - D-0653-2016 Feb 17, 2016 · Class II
Presence of Foreign Tablets/Capsules: Presence of a comingled Carbimazole 5 mg tablet.
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