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TIOPRONIN

NDC 13668-692, tiopronin, tablet, delayed release, from Torrent Pharmaceuticals Limited.

Product NDC
13668-692
Status
Listed
Labeler
Torrent Pharmaceuticals Limited
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/13668-692 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TIOPRONIN300 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
13668-692-901366806929090 TABLET, DELAYED RELEASE in 1 BOTTLE (13668-692-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ad750031-08ec-4d92-af2d-97a80c454e14

Use it

Look up 13668-692 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/13668-692 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 13668-692. 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.