NDC 16729-235 – ropinirole
Ropinirole Hydrochloride 2 mg/1 · Tablet, Film Coated · Oral
Product NDC16729-235
Product details
- Brand name
- ropinirole
- Generic name
- ropinirole
- Labeler
- Accord Healthcare Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA204022
- Marketed since
- October 17, 2018
- Listing expires
- December 31, 2026
- Pharmacologic class
- Nonergot Dopamine Agonist
Active ingredients
- Ropinirole Hydrochloride 2 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 16729-235-01 | 100 TABLET, FILM COATED in 1 BOTTLE (16729-235-01) | Oct 17, 2018 |
Recalls mentioning this NDC
- D-0430-2023 Mar 8, 2023 · Class II
CGMP Deviations: recalling drug products following an FDA inspection. - D-0425-2023 Mar 8, 2023 · Class II
CGMP Deviations: recalling drug products following an FDA inspection. - D-0431-2023 Mar 8, 2023 · Class II
CGMP Deviations: recalling drug products following an FDA inspection. - D-0429-2023 Mar 8, 2023 · Class II
CGMP Deviations: recalling drug products following an FDA inspection. - D-0428-2023 Mar 8, 2023 · Class II
CGMP Deviations: recalling drug products following an FDA inspection. - D-0427-2023 Mar 8, 2023 · Class II
CGMP Deviations: recalling drug products following an FDA inspection. - D-0426-2023 Mar 8, 2023 · Class II
CGMP Deviations: recalling drug products following an FDA inspection.
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- 16729-236 Ropinirole Hydrochloride 3 mg/1 · Tablet, Film Coated · Accord Healthcare Inc.
- 16729-234 Ropinirole Hydrochloride 1 mg/1 · Tablet, Film Coated · Accord Healthcare Inc.
- 16729-233 Ropinirole Hydrochloride .5 mg/1 · Tablet, Film Coated · Accord Healthcare Inc.
- 16729-238 Ropinirole Hydrochloride 5 mg/1 · Tablet, Film Coated · Accord Healthcare Inc.
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