Paliperidone
- Product NDC
- 10147-0952
- 11-digit product format
- 101470952
- Labeler code
- 10147
- Product ID
- 10147-0952_ef450fb4-b6a3-11ec-b9d7-d1fdddc23fea
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- paliperidone
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Patriot Pharmaceuticals, LLC
- Application
- NDA021999
- Marketing category
- NDA
- Marketing start
- 2015-09-24
- Marketing end
- 0000-00-00
- Substance
- PALIPERIDONE
- Active strength
- 3 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [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 |
|---|
| 10147-0952-1 | 10147095201 | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (10147-0952-1) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 10 blister pack | 2015-09-24 | 0000-00-00 | No | No | Current |
| 10147-0952-3 | 10147095203 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (10147-0952-3) | | 2015-09-24 | 0000-00-00 | No | No | Current |