Losartan Potassium
- Product NDC
- 71335-1582
- 11-digit product format
- 713351582
- Labeler code
- 71335
- Product ID
- 71335-1582_ee7edcfc-8787-49ba-810c-6c4f5d5fa8df
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA203835
- Marketing category
- ANDA
- Marketing start
- 2015-08-19
- 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 |
|---|
| 71335-1582-1 | 71335158201 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1582-1) | 2020-04-30 | No | No | Historical |
| 71335-1582-2 | 71335158202 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1582-2) | 2020-04-30 | No | No | Historical |
| 71335-1582-3 | 71335158203 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1582-3) | 2020-04-30 | No | No | Historical |
| 71335-1582-4 | 71335158204 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-1582-4) | 2020-04-30 | No | No | Historical |
| 71335-1582-5 | 71335158205 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-1582-5) | 2020-04-30 | No | No | Historical |
| 71335-1582-6 | 71335158206 | 7 TABLET, FILM COATED in 1 BOTTLE (71335-1582-6) | 2020-04-30 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Losartan Potassium | Bryant Ranch Prepack | 2024-08-26 | Human Prescription Drug Label | 6 |