Losartan potassium
- Product NDC
- 67046-1510
- 11-digit product format
- 670461510
- Labeler code
- 67046
- Product ID
- 67046-1510_2d1ad3cf-2474-bcba-e063-6294a90a6054
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Coupler LLC
- Application
- ANDA202230
- Marketing category
- ANDA
- Marketing start
- 2025-02-01
- Substance
- LOSARTAN POTASSIUM
- Active strength
- 50 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 3ST302B24A | LOSARTAN POTASSIUM | 124750-99-8 | LOSARTAN POTASSIUM |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 67046-1510-3 | 67046151003 | 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1510-3) | 2025-02-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Losartan potassium | Coupler LLC | 2025-02-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |