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CYPROHEPTADINE HYDROCHLORIDE

NDC 70710-1110, CYPROHEPTADINE HYDROCHLORIDE, tablet, from Zydus Pharmaceuticals USA Inc..

Product NDC
70710-1110
Status
Listed
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208938
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1110 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CYPROHEPTADINE HYDROCHLORIDE4 mg/1
Package NDCNDC-11Package
70710-1110-0707101110001000 TABLET in 1 BOTTLE (70710-1110-0)
70710-1110-170710111001100 TABLET in 1 BOTTLE (70710-1110-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/766f9b59-2c72-45ac-af09-5dd6c3e16b52

  • NADAC price for package 70710111000

    GET /v1/drugs/nadac/70710111000

  • NADAC price for package 70710111001

    GET /v1/drugs/nadac/70710111001

Use it

Look up 70710-1110 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1110 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70710-1110. 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.