Olmesartan Medoxomil and Hydrochlorothiazide
NDC 71335-2180, Olmesartan Medoxomil and Hydrochlorothiazide, tablet, from Bryant Ranch Prepack.
- Product NDC
- 71335-2180
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA208847
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2180 \ -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 |
|---|---|---|
| 71335-2180-1 | 71335218001 | 30 TABLET in 1 BOTTLE (71335-2180-1) |
| 71335-2180-2 | 71335218002 | 90 TABLET in 1 BOTTLE (71335-2180-2) |
| 71335-2180-3 | 71335218003 | 28 TABLET in 1 BOTTLE (71335-2180-3) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/77e71a2e-8370-4f7a-a5e4-93d86bd37dad
Use it
Look up 71335-2180 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2180 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71335-2180. 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.