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VENXXIVA

NDC 70709-121, tiopronin, tablet, delayed release, from Cycle Pharmaceuticals Ltd..

Product NDC
70709-121
Status
Listed
Labeler
Cycle Pharmaceuticals Ltd.
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216990
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70709-121 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TIOPRONIN100 mg/1

Pharmacologic classes

Cystine Disulfide Reduction [MoA]; N-substituted Glycines [CS]; Reducing and Complexing Thiol [EPC]

Package NDCNDC-11Package
70709-121-3070709012130300 TABLET, DELAYED RELEASE in 1 BOTTLE (70709-121-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/02e24443-04c6-4b98-a395-49aec4a468de

Use it

Look up 70709-121 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70709-121 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70709-121. 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.