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CYPROHEPTADINE HYDROCHLORIDE

NDC 50742-190, CYPROHEPTADINE HYDROCHLORIDE, tablet, from Ingenus Pharmaceuticals LLC.

Product NDC
50742-190
Status
Listed
Labeler
Ingenus Pharmaceuticals LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA205087
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50742-190 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CYPROHEPTADINE HYDROCHLORIDE4 mg/1
Package NDCNDC-11Package
50742-190-0150742019001100 TABLET in 1 BOTTLE, PLASTIC (50742-190-01)
50742-190-10507420190101000 TABLET in 1 BOTTLE, PLASTIC (50742-190-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/56f428c9-8d33-4c91-91d8-1fe194335066

  • NADAC price for package 50742019001

    GET /v1/drugs/nadac/50742019001

Use it

Look up 50742-190 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50742-190 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50742-190. 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.