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Fluphenazine Hydrochloride

NDC 70710-1488, Fluphenazine Hydrochloride, tablet, film coated, from Zydus Pharmaceuticals (USA) Inc..

Product NDC
70710-1488
Status
Listed
Labeler
Zydus Pharmaceuticals (USA) Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214552
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1488 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FLUPHENAZINE HYDROCHLORIDE1 mg/1

Pharmacologic classes

Phenothiazine [EPC]; Phenothiazines [CS]

Package NDCNDC-11Package
70710-1488-170710148801100 TABLET, FILM COATED in 1 BOTTLE (70710-1488-1)
70710-1488-570710148805500 TABLET, FILM COATED in 1 BOTTLE (70710-1488-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c4448579-3ccb-442e-8950-a219d1f01a98

Use it

Look up 70710-1488 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1488 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70710-1488. 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.