PRAMIPEXOLE DIHYDROCHLORIDE
- Product NDC
- 65841-735
- 11-digit product format
- 658410735
- Labeler code
- 65841
- Product ID
- 65841-735_45a8b1f5-90da-46df-9f01-2f174331f3e8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PRAMIPEXOLE DIHYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA078920
- Marketing category
- ANDA
- Marketing start
- 2010-07-10
- Marketing end
- 0000-00-00
- Substance
- PRAMIPEXOLE DIHYDROCHLORIDE
- Active strength
- 0 mg/1
- Pharmacologic classes
- Dopamine Agonists [MoA], Nonergot Dopamine Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 65841-735-05 | 65841073505 | 500 TABLET in 1 BOTTLE (65841-735-05) | 500 tablet | 2010-07-10 | 0000-00-00 | No | No | Current |
| 65841-735-10 | 65841073510 | 1000 TABLET in 1 BOTTLE (65841-735-10) | 1000 tablet | 2010-07-10 | 0000-00-00 | No | No | Current |
| 65841-735-16 | 65841073516 | 90 TABLET in 1 BOTTLE (65841-735-16) | 90 tablet | 2010-07-10 | 0000-00-00 | No | No | Current |