Losartan Potassium
- Product NDC
- 71610-083
- 11-digit product format
- 716100083
- Labeler code
- 71610
- Product ID
- 71610-083_231334fb-3368-46d4-80a2-737fda561a05
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA090083
- Marketing category
- ANDA
- Marketing start
- 2010-10-06
- 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 |
|---|
| 71610-083-30 | 71610008330 | 30 TABLET, FILM COATED in 1 BOTTLE (71610-083-30) | 2018-06-27 | No | No | Historical |
| 71610-083-60 | 71610008360 | 90 TABLET, FILM COATED in 1 BOTTLE (71610-083-60) | 2018-06-06 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Losartan Potassium | Aphena Pharma Solutions - Tennessee, LLC | 2018-07-09 | Human Prescription Drug Label | 1 |