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CYPROHEPTADINE HYDROCHLORIDE

NDC 70771-1076, CYPROHEPTADINE HYDROCHLORIDE, tablet, from Zydus Lifesciences Limited.

Product NDC
70771-1076
Status
Listed
Labeler
Zydus Lifesciences Limited
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/70771-1076 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CYPROHEPTADINE HYDROCHLORIDE4 mg/1
Package NDCNDC-11Package
70771-1076-0707711076001000 TABLET in 1 BOTTLE (70771-1076-0)
70771-1076-170771107601100 TABLET in 1 BOTTLE (70771-1076-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ccd7d3b2-b0c1-4f66-8d06-d21f5cfa8c1e

Use it

Look up 70771-1076 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1076 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1076. 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.