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Nitazoxanide

NDC 70954-934, Nitazoxanide, tablet, from ANI Pharmaceuticals, Inc..

Product NDC
70954-934
Status
Listed
Labeler
ANI Pharmaceuticals, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214844
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70954-934 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NITAZOXANIDE500 mg/1

Pharmacologic classes

Antiprotozoal [EPC]

Package NDCNDC-11Package
70954-934-10709540934106 TABLET in 1 BOTTLE (70954-934-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/cd3652fa-a183-4fb6-9a21-73fbeba6fc4b

  • NADAC price for package 70954093410

    GET /v1/drugs/nadac/70954093410

Use it

Look up 70954-934 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70954-934 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70954-934. 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.