Fluphenazine Hydrochloride
NDC 0121-0654, Fluphenazine Hydrochloride, elixir, from PAI Holdings, LLC dba PAI Pharma.
- Product NDC
- 0121-0654
- Status
- Listed
- Labeler
- PAI Holdings, LLC dba PAI Pharma
- Dosage form
- ELIXIR
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA040146
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0121-0654 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FLUPHENAZINE HYDROCHLORIDE.5 mg/mL
Pharmacologic classes
Phenothiazine [EPC]; Phenothiazines [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0121-0654-02 | 00121065402 | 60 mL in 1 BOTTLE (0121-0654-02) |
| 0121-0654-16 | 00121065416 | 473 mL in 1 BOTTLE (0121-0654-16) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/f0a89d5d-01db-47f3-a873-33ab49c6e4f8
Use it
Look up 0121-0654 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0121-0654 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0121-0654. 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.