Fluphenazine Hydrochloride
NDC 70954-274, Fluphenazine Hydrochloride, tablet, from ANI Pharmaceuticals, Inc..
- Product NDC
- 70954-274
- Status
- Listed
- Labeler
- ANI Pharmaceuticals, Inc.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA214674
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70954-274 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FLUPHENAZINE HYDROCHLORIDE2.5 mg/1
Pharmacologic classes
Phenothiazine [EPC]; Phenothiazines [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70954-274-10 | 70954027410 | 100 TABLET in 1 BOTTLE (70954-274-10) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/6218cbd2-1f7f-40fa-92d2-5d5b0d7fa60bNADAC price for package 70954027410
GET /v1/drugs/nadac/70954027410
Use it
Look up 70954-274 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70954-274 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70954-274. 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.