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Ivermectin

NDC 70771-1731, Ivermectin, tablet, from Zydus Lifesciences Limited.

Product NDC
70771-1731
Status
Listed
Labeler
Zydus Lifesciences Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216863
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1731 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • IVERMECTIN3 mg/1

Pharmacologic classes

Antiparasitic [EPC]; Pediculicide [EPC]

Package NDCNDC-11Package
70771-1731-3707711731032 BLISTER PACK in 1 CARTON (70771-1731-3) / 10 TABLET in 1 BLISTER PACK (70771-1731-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6d626814-5288-441c-9508-f7f5130feceb

Use it

Look up 70771-1731 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1731 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1731. 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.