Losartan Potassium
- Product NDC
- 63187-708
- 11-digit product format
- 631870708
- Labeler code
- 63187
- Product ID
- 63187-708_e7f9bccb-bb82-49fd-b59b-92670ee46f9e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA203835
- Marketing category
- ANDA
- Marketing start
- 2015-08-19
- 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 |
|---|
| 63187-708-30 | 63187070830 | 30 TABLET, FILM COATED in 1 BOTTLE (63187-708-30) | 2016-06-01 | No | No | Historical |
| 63187-708-60 | 63187070860 | 60 TABLET, FILM COATED in 1 BOTTLE (63187-708-60) | 2016-06-01 | No | No | Historical |
| 63187-708-90 | 63187070890 | 90 TABLET, FILM COATED in 1 BOTTLE (63187-708-90) | 2016-06-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Losartan Potassium | Proficient Rx LP | 2022-08-01 | HUMAN PRESCRIPTION DRUG LABEL | 4 |