Paliperidone
- Product NDC
- 42292-026
- 11-digit product format
- 422920026
- Labeler code
- 42292
- Product ID
- 42292-026_f0e73f03-8af4-d75f-e053-2995a90ae6f8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- paliperidone
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA203802
- Marketing category
- ANDA
- Marketing start
- 2016-09-20
- Marketing end
- 2023-11-29
- Substance
- PALIPERIDONE
- Active strength
- 3 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 42292-026-20 | 42292002620 | 100 BLISTER PACK in 1 CARTON (42292-026-20) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (42292-026-01) | 100 blister pack | 2016-09-20 | 0000-00-00 | No | No | Current |