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Cyproheptadine Hydrochloride

NDC 42708-177, Cyproheptadine Hydrochloride, tablet, from QPharma Inc.

Product NDC
42708-177
Status
Listed
Labeler
QPharma Inc
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206553
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42708-177 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CYPROHEPTADINE HYDROCHLORIDE4 mg/1
Package NDCNDC-11Package
42708-177-214270801772121 TABLET in 1 BOTTLE, PLASTIC (42708-177-21)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/fc75bd79-63b7-6388-e053-6394a90ac377

Use it

Look up 42708-177 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42708-177 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42708-177. 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.