NDC 46708-264 – Ropinirole
Ropinirole Hydrochloride 6 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC46708-264
Product details
- Brand name
- Ropinirole
- Generic name
- Ropinirole
- Labeler
- Alembic Pharmaceuticals Limited
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA202786
- Marketed since
- March 14, 2013
- Listing expires
- December 31, 2026
- Pharmacologic class
- Nonergot Dopamine Agonist
Active ingredients
- Ropinirole Hydrochloride 6 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 46708-264-10 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 CARTON (46708-264-10) | Mar 14, 2013 |
| 46708-264-30 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-264-30) | Mar 14, 2013 |
| 46708-264-31 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-264-31) | Mar 14, 2013 |
| 46708-264-71 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-264-71) | Mar 14, 2013 |
| 46708-264-90 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-264-90) | Mar 14, 2013 |
| 46708-264-91 | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-264-91) | Mar 14, 2013 |
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