OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE
NDC 50228-343, OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE, tablet, film coated, from ScieGen Pharmaceuticals Inc.
- Product NDC
- 50228-343
- Status
- Listed
- Labeler
- ScieGen Pharmaceuticals Inc
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA208465
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/50228-343 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- OLMESARTAN MEDOXOMIL40 mg/1
- HYDROCHLOROTHIAZIDE12.5 mg/1
Pharmacologic classes
Angiotensin 2 Receptor Antagonists [MoA]; Angiotensin 2 Receptor Blocker [EPC]; Increased Diuresis [PE]; Thiazide Diuretic [EPC]; Thiazides [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 50228-343-10 | 50228034310 | 1000 TABLET, FILM COATED in 1 BOTTLE (50228-343-10) |
| 50228-343-30 | 50228034330 | 30 TABLET, FILM COATED in 1 BOTTLE (50228-343-30) |
| 50228-343-90 | 50228034390 | 90 TABLET, FILM COATED in 1 BOTTLE (50228-343-90) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/52332190-2a12-d205-e063-6394a90ab7c5
Use it
Look up 50228-343 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/50228-343 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 50228-343. 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.