Losartan Potassium and Hydrochlorothiazide
NDC 71335-0152, Losartan Potassium and Hydrochlorothiazide, tablet, film coated, from Bryant Ranch Prepack.
- Product NDC
- 71335-0152
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA091629
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0152 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- LOSARTAN POTASSIUM50 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 |
|---|---|---|
| 71335-0152-1 | 71335015201 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0152-1) |
| 71335-0152-2 | 71335015202 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0152-2) |
| 71335-0152-3 | 71335015203 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0152-3) |
| 71335-0152-4 | 71335015204 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-0152-4) |
| 71335-0152-5 | 71335015205 | 58 TABLET, FILM COATED in 1 BOTTLE (71335-0152-5) |
| 71335-0152-6 | 71335015206 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-0152-6) |
| 71335-0152-7 | 71335015207 | 180 TABLET, FILM COATED in 1 BOTTLE (71335-0152-7) |
| 71335-0152-8 | 71335015208 | 1000 TABLET, FILM COATED in 1 BOTTLE (71335-0152-8) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/60f3f17d-fd28-406d-97ca-9f01f5f1c72c
Use it
Look up 71335-0152 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0152 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71335-0152. 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.