NDC 72189-222 – Ropinirole
Ropinirole Hydrochloride 1 mg/1 · Tablet, Film Coated · Oral
Product NDC72189-222
Product details
- Brand name
- Ropinirole
- Generic name
- Ropinirole
- Labeler
- DIRECT RX
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA204022
- Marketed since
- May 20, 2021
- Listing expires
- December 31, 2026
- Pharmacologic class
- Nonergot Dopamine Agonist
Active ingredients
- Ropinirole Hydrochloride 1 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 72189-222-30 | 30 TABLET, FILM COATED in 1 BOTTLE (72189-222-30) | May 20, 2021 |
| 72189-222-60 | 60 TABLET, FILM COATED in 1 BOTTLE (72189-222-60) | May 20, 2021 |
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