Fluphenazine Hydrochloride
NDC 0832-6003, Fluphenazine Hydrochloride, tablet, film coated, from Upsher-Smith Laboratories,LLC.
- Product NDC
- 0832-6003
- Status
- Listed
- Labeler
- Upsher-Smith Laboratories,LLC
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA213784
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0832-6003 \ -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 |
|---|
Linked data
RxNorm, label and prices
RxNorm concepts
RxNorm links no concept to this product's packages.
Related lookups
FDA label sections
GET /v1/drugs/labels/f07bb3f1-c68c-441b-9de4-99a219f2500a
Use it
Look up 0832-6003 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0832-6003 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0832-6003. 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.