Losartan Potassium
- Product NDC
- 72189-303
- 11-digit product format
- 721890303
- Labeler code
- 72189
- Product ID
- 72189-303_2c295943-f8ca-fd38-e063-6394a90ad5cf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- DirectRx
- Application
- ANDA203835
- Marketing category
- ANDA
- Marketing start
- 2021-12-17
- Substance
- LOSARTAN POTASSIUM
- Active strength
- 25 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 |
|---|
| 72189-303-90 | 72189030390 | 90 TABLET, FILM COATED in 1 BOTTLE (72189-303-90) | 2021-12-17 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Losartan Potassium | DirectRx | 2025-01-20 | HUMAN PRESCRIPTION DRUG LABEL | 2 |