Losartan Potassium and Hydrochlorothiazide
NDC 82804-103, losartan potassium and hydrochlorothiazide, tablet, film coated, from Proficient Rx LP.
- Product NDC
- 82804-103
- Status
- Listed
- Labeler
- Proficient Rx LP
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA204901
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/82804-103 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- LOSARTAN POTASSIUM100 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 |
|---|---|---|
| 82804-103-90 | 82804010390 | 90 TABLET, FILM COATED in 1 BOTTLE (82804-103-90) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/c6ed6f74-0eca-4f99-8c7e-dd3f56167f01
Use it
Look up 82804-103 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/82804-103 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 82804-103. 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.