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Cyproheptadine Hydrochloride

NDC 72789-102, Cyproheptadine Hydrochloride, tablet, from PD-Rx Pharmaceuticals, Inc..

Product NDC
72789-102
Status
Listed
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206676
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72789-102 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CYPROHEPTADINE HYDROCHLORIDE4 mg/1
Package NDCNDC-11Package
72789-102-0172789010201100 TABLET in 1 BOTTLE, PLASTIC (72789-102-01)
72789-102-307278901023030 TABLET in 1 BOTTLE, PLASTIC (72789-102-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/03e69414-8a25-4ed8-b7ac-16445b879b1f

Use it

Look up 72789-102 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72789-102 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72789-102. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.