Losartan Potassium
- Product NDC
- 68071-3846
- 11-digit product format
- 680713846
- Labeler code
- 68071
- Product ID
- 68071-3846_351d4de0-4f1e-9ac7-e063-6394a90a6b21
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals.Inc.
- Application
- ANDA091497
- Marketing category
- ANDA
- Marketing start
- 2022-03-20
- Substance
- LOSARTAN POTASSIUM
- Active strength
- 100 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 |
|---|
| 68071-3846-3 | 68071384603 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-3846-3) | 2025-05-14 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Losartan Potassium | NuCare Pharmaceuticals.Inc. | 2025-05-14 | HUMAN PRESCRIPTION DRUG LABEL | 1 |