IRBESARTAN
NDC 42658-121, IRBESARTAN, tablet, film coated, from Hisun Pharmaceuticals USA Inc..
- Product NDC
- 42658-121
- Status
- Listed
- Labeler
- Hisun Pharmaceuticals USA Inc.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA206194
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/42658-121 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- IRBESARTAN75 mg/1
Pharmacologic classes
Angiotensin 2 Receptor Antagonists [MoA]; Angiotensin 2 Receptor Blocker [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 42658-121-01 | 42658012101 | 30 TABLET, FILM COATED in 1 BOTTLE (42658-121-01) |
| 42658-121-04 | 42658012104 | 90 TABLET, FILM COATED in 1 BOTTLE (42658-121-04) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/61ab1b6e-c849-49ca-a3f0-150774db649d
Use it
Look up 42658-121 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/42658-121 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 42658-121. 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.