OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE
NDC 71335-9686, olmesartan medoxomil and hydrochlorothiazide, tablet, from Bryant Ranch Prepack.
- Product NDC
- 71335-9686
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA207804
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71335-9686 \ -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 |
|---|---|---|
| 71335-9686-1 | 71335968601 | 30 TABLET in 1 BOTTLE (71335-9686-1) |
| 71335-9686-2 | 71335968602 | 90 TABLET in 1 BOTTLE (71335-9686-2) |
| 71335-9686-3 | 71335968603 | 28 TABLET in 1 BOTTLE (71335-9686-3) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/2c8bb018-af07-4745-a4e9-f9a6795a5ea2
Use it
Look up 71335-9686 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71335-9686 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71335-9686. 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.