ROPINIROLE
- Product NDC
- 61919-780
- 11-digit product format
- 619190780
- Labeler code
- 61919
- Product ID
- 61919-780_cc0df9b3-16e9-d642-e053-2a95a90a7726
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ROPINIROLE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA090429
- Marketing category
- ANDA
- Marketing start
- 2019-01-14
- Marketing end
- 0000-00-00
- Substance
- ROPINIROLE HYDROCHLORIDE
- Active strength
- 3 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-780-30 | 61919078030 | 30 TABLET, FILM COATED in 1 BOTTLE (61919-780-30) | 2019-01-14 | 0000-00-00 | No | No | Current |
| 61919-780-90 | 61919078090 | 30 TABLET, FILM COATED in 1 BOTTLE (61919-780-90) | 2019-01-14 | 0000-00-00 | No | No | Current |