Paliperidone
NDC 16714-867, Paliperidone, tablet, film coated, extended release, from NorthStar RxLLC.
- Product NDC
- 16714-867
- Status
- Listed
- Labeler
- NorthStar RxLLC
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA205618
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/16714-867 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PALIPERIDONE3 mg/1
Pharmacologic classes
Atypical Antipsychotic [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 16714-867-01 | 16714086701 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (16714-867-01) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/5589ec69-c49c-44a7-9561-bbffeb918d1fNADAC price for package 16714086701
GET /v1/drugs/nadac/16714086701
Use it
Look up 16714-867 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/16714-867 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 16714-867. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.