Fluphenazine Hydrochoride
NDC 16571-889, fluphenazine hydrochloride, tablet, film coated, from Rising Pharma Holdings, Inc..
- Product NDC
- 16571-889
- Status
- Listed
- Labeler
- Rising Pharma Holdings, Inc.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA218283
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/16571-889 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FLUPHENAZINE HYDROCHLORIDE1 mg/1
Pharmacologic classes
Phenothiazine [EPC]; Phenothiazines [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 16571-889-09 | 16571088909 | 90 TABLET, FILM COATED in 1 CONTAINER (16571-889-09) |
| 16571-889-50 | 16571088950 | 500 TABLET, FILM COATED in 1 CONTAINER (16571-889-50) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/9fd44ab9-79bb-472e-8434-c3d786b42de5NADAC price for package 16571088909
GET /v1/drugs/nadac/16571088909
Use it
Look up 16571-889 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/16571-889 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 16571-889. 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.