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tiopronin

NDC 60219-2009, tiopronin, tablet, delayed release, from Amneal Pharmaceuticals NY LLC.

Product NDC
60219-2009
Status
Listed
Labeler
Amneal Pharmaceuticals NY LLC
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216278
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/60219-2009 \
  -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
60219-2009-96021920090990 TABLET, DELAYED RELEASE in 1 BOTTLE (60219-2009-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ce5b1f97-5b3c-40b6-b1c4-1d36025be1b8

Use it

Look up 60219-2009 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/60219-2009 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 60219-2009. 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.