NDC 87063-199 – Ropinirole
Ropinirole Hydrochloride .5 mg/1 · Tablet, Film Coated · Oral
Product NDC87063-199
Product details
- Brand name
- Ropinirole
- Generic name
- Ropinirole
- Labeler
- ASCLEMED USA INC.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA079229
- Marketed since
- September 15, 2022
- Listing expires
- December 31, 2027
- Pharmacologic class
- Nonergot Dopamine Agonist
Active ingredients
- Ropinirole Hydrochloride .5 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 87063-199-01 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-199-01) | May 7, 2026 |
| 87063-199-30 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-199-30) | May 7, 2026 |
| 87063-199-60 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-199-60) | May 7, 2026 |
| 87063-199-90 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-199-90) | May 7, 2026 |
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