Losartan Potassium
- Product NDC
- 71205-226
- 11-digit product format
- 712050226
- Labeler code
- 71205
- Product ID
- 71205-226_61dad858-613a-4add-a885-b63adc2048ba
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA091497
- Marketing category
- ANDA
- Marketing start
- 2011-06-01
- 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 |
|---|
| 71205-226-30 | 71205022630 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-226-30) | 2019-02-01 | No | No | Historical |
| 71205-226-60 | 71205022660 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-226-60) | 2019-02-01 | No | No | Historical |
| 71205-226-90 | 71205022690 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-226-90) | 2019-02-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Losartan Potassium | Proficient Rx LP | 2022-07-01 | HUMAN PRESCRIPTION DRUG LABEL | 3 |