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Fluphenazine Hydrochloride

NDC 68462-914, Fluphenazine Hydrochloride, tablet, film coated, from Glenmark Pharmaceuticals Inc., USA.

Product NDC
68462-914
Status
Listed
Labeler
Glenmark Pharmaceuticals Inc., USA
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216350
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68462-914 \
  -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
68462-914-0168462091401100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68462-914-01)
68462-914-0568462091405500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68462-914-05)
68462-914-1468462091414100 BLISTER PACK in 1 CARTON (68462-914-14) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4c3eea71-a7a1-4eda-9871-034ddeb83ed6

Use it

Look up 68462-914 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68462-914 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68462-914. 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.