NDC 68462-255 – Ropinirole
Ropinirole Hydrochloride 1 mg/1 · Tablet, Film Coated · Oral
Product NDC68462-255
Product details
- Brand name
- Ropinirole
- Generic name
- Ropinirole
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA090135
- Marketed since
- February 25, 2010
- Listing expires
- December 31, 2027
- Pharmacologic class
- Nonergot Dopamine Agonist
Active ingredients
- Ropinirole Hydrochloride 1 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 68462-255-01 | 100 TABLET, FILM COATED in 1 BOTTLE (68462-255-01) | Feb 25, 2010 |
| 68462-255-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (68462-255-10) | Feb 25, 2010 |
| 68462-255-11 | 10 BLISTER PACK in 1 CARTON (68462-255-11) / 10 TABLET, FILM COATED in 1 BLISTER PACK | Feb 25, 2010 |
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