Ethambutol Hydrochloride
NDC 54879-001, Ethambutol Hydrochloride, tablet, film coated, from STI Pharma LLC.
- Product NDC
- 54879-001
- Status
- Listed
- Labeler
- STI Pharma LLC
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA AUTHORIZED GENERIC
- Application
- NDA016320
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/54879-001 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ETHAMBUTOL HYDROCHLORIDE100 mg/1
Pharmacologic classes
Antimycobacterial [EPC]
| Package NDC | NDC-11 | Package |
|---|
Linked data
RxNorm, label and prices
RxNorm concepts
RxNorm links no concept to this product's packages.
Related lookups
FDA label sections
GET /v1/drugs/labels/3f6428d6-3745-4337-ad78-ebfff9f49135
Use it
Look up 54879-001 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/54879-001 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 54879-001. 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.