Pramipexole dihydrochloride
- Product NDC
- 50090-2217
- 11-digit product format
- 500902217
- Labeler code
- 50090
- Product ID
- 50090-2217_dcdcf439-fbb9-4bd0-a5e5-f2ee87add044
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pramipexole dihydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA090781
- Marketing category
- ANDA
- Marketing start
- 2010-10-08
- Marketing end
- 0000-00-00
- Substance
- PRAMIPEXOLE DIHYDROCHLORIDE
- 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 3D867NP06J | PRAMIPEXOLE DIHYDROCHLORIDE | 191217-81-9 | PRAMIPEXOLE DIHYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-2217-0 | 50090221700 | 30 TABLET in 1 BOTTLE (50090-2217-0) | 30 tablet | 2015-11-03 | 0000-00-00 | No | No | Current |