Losartan potassium Tablets, 100 mg
- Product NDC
- 72162-1698
- 11-digit product format
- 721621698
- Labeler code
- 72162
- Product ID
- 72162-1698_479a9534-5c54-4a49-8656-08897c62a73d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- losartan potassium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA201170
- Marketing category
- ANDA
- Marketing start
- 2012-09-18
- 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 | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1698-0 | 72162169800 | 1000 TABLET in 1 BOTTLE (72162-1698-0) | 1000 tablet | 2024-02-06 | No | No | Historical |