Thiola EC
NDC 0178-0901, tiopronin, tablet, delayed release, from Mission Pharmacal Company.
- Product NDC
- 0178-0901
- Status
- Listed
- Labeler
- Mission Pharmacal Company
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA211843
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0178-0901 \ -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 NDC | NDC-11 | Package |
|---|---|---|
| 0178-0901-90 | 00178090190 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (0178-0901-90) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/20298a52-a194-a161-8632-d84b6f26e23c
Use it
Look up 0178-0901 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0178-0901 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0178-0901. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.