Ropinirole Hydrochloride
- Product NDC
- 60429-822
- 11-digit product format
- 604290822
- Labeler code
- 60429
- Product ID
- 60429-822_d0129390-da28-5cdf-e053-2a95a90ac50e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ropinirole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA078881
- Marketing category
- ANDA
- Marketing start
- 2008-05-05
- Marketing end
- 0000-00-00
- Substance
- ROPINIROLE HYDROCHLORIDE
- Active strength
- 4 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60429-822-01 | 60429082201 | 100 TABLET in 1 BOTTLE, PLASTIC (60429-822-01) | 100 tablet | 2016-06-20 | 0000-00-00 | No | No | Current |