Fluphenazine Hydrochloride
NDC 59651-688, Fluphenazine Hydrochloride, tablet, from Aurobindo Pharma Limited.
- Product NDC
- 59651-688
- Status
- Listed
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA218055
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/59651-688 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FLUPHENAZINE HYDROCHLORIDE5 mg/1
Pharmacologic classes
Phenothiazine [EPC]; Phenothiazines [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 59651-688-01 | 59651068801 | 100 TABLET in 1 BOTTLE (59651-688-01) |
| 59651-688-05 | 59651068805 | 500 TABLET in 1 BOTTLE (59651-688-05) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/e73764e7-e666-4ad3-a029-04a528dc1c9eNADAC price for package 59651068801
GET /v1/drugs/nadac/59651068801
Use it
Look up 59651-688 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/59651-688 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 59651-688. 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.