ropinirole
- Product NDC
- 70518-2439
- 11-digit product format
- 705182439
- Labeler code
- 70518
- Product ID
- 70518-2439_c936a711-6bba-d89b-e053-2a95a90af0cd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ropinirole
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA204022
- Marketing category
- ANDA
- Marketing start
- 2019-11-20
- Marketing end
- 0000-00-00
- Substance
- ROPINIROLE HYDROCHLORIDE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2439-0 | 70518243900 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2439-0) | 2019-11-20 | 0000-00-00 | No | No | Current |
| 70518-2439-1 | 70518243901 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2439-1) | 2020-01-25 | 0000-00-00 | No | No | Current |