Losartan Potassium
NDC 68071-3846, Losartan Potassium, tablet, film coated, from NuCare Pharmaceuticals.Inc..
- Product NDC
- 68071-3846
- Status
- Listed
- Labeler
- NuCare Pharmaceuticals.Inc.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA091497
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/68071-3846 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- LOSARTAN POTASSIUM100 mg/1
Pharmacologic classes
Angiotensin 2 Receptor Antagonists [MoA]; Angiotensin 2 Receptor Blocker [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 68071-3846-3 | 68071384603 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-3846-3) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/351d3c5c-05c6-921a-e063-6394a90abef9
Use it
Look up 68071-3846 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68071-3846 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68071-3846. 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.