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Fluphenazine Hydrochloride

NDC 51672-4236, Fluphenazine Hydrochloride, tablet, film coated, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-4236
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215674
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4236 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FLUPHENAZINE HYDROCHLORIDE10 mg/1

Pharmacologic classes

Phenothiazine [EPC]; Phenothiazines [CS]

Package NDCNDC-11Package
51672-4236-151672423601100 TABLET, FILM COATED in 1 BOTTLE (51672-4236-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7036f7c6-0792-400d-a1c7-54f21b2bd481

  • NADAC price for package 51672423601

    GET /v1/drugs/nadac/51672423601

Use it

Look up 51672-4236 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4236 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-4236. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.