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Raloxifene hydrochloride

NDC 50228-306, Raloxifene hydrochloride, tablet, film coated, from ScieGen Pharmaceuticals Inc.

Product NDC
50228-306
Status
Listed
Labeler
ScieGen Pharmaceuticals Inc
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206384
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50228-306 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • RALOXIFENE HYDROCHLORIDE60 mg/1

Pharmacologic classes

Estrogen Agonist/Antagonist [EPC]; Selective Estrogen Receptor Modulators [MoA]

Package NDCNDC-11Package
50228-306-20502280306202000 TABLET, FILM COATED in 1 BOTTLE (50228-306-20)
50228-306-305022803063030 TABLET, FILM COATED in 1 BOTTLE (50228-306-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8152e68b-61a8-4897-8e03-900135b1dbd5

Use it

Look up 50228-306 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50228-306 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50228-306. 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.