Pramipexole dihydrochloride
- Product NDC
- 71335-1112
- 11-digit product format
- 713351112
- Labeler code
- 71335
- Product ID
- 71335-1112_1cf5237d-656b-45a4-8486-317ff86f080e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pramipexole dihydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA202164
- Marketing category
- ANDA
- Marketing start
- 2012-09-21
- 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
- 2020-12-31
- 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 |
|---|
| 71335-1112-1 | 71335111201 | 90 TABLET in 1 BOTTLE (71335-1112-1) | 90 tablet | 2014-04-07 | 0000-00-00 | No | No | Current |
| 71335-1112-2 | 71335111202 | 30 TABLET in 1 BOTTLE (71335-1112-2) | 30 tablet | 2014-04-07 | 0000-00-00 | No | No | Current |
| 71335-1112-3 | 71335111203 | 60 TABLET in 1 BOTTLE (71335-1112-3) | 60 tablet | 2014-04-07 | 0000-00-00 | No | No | Current |