Losartan Potassium
- Product NDC
- 63187-357
- 11-digit product format
- 631870357
- Labeler code
- 63187
- Product ID
- 63187-357_6d496790-edf8-4309-bc31-2700e9a8c84d
- 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
- 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 |
|---|
| 63187-357-30 | 63187035730 | 30 TABLET, FILM COATED in 1 BOTTLE (63187-357-30) | 2016-08-01 | No | No | Historical |
| 63187-357-60 | 63187035760 | 60 TABLET, FILM COATED in 1 BOTTLE (63187-357-60) | 2016-08-01 | No | No | Historical |
| 63187-357-90 | 63187035790 | 90 TABLET, FILM COATED in 1 BOTTLE (63187-357-90) | 2016-08-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Losartan Potassium | Proficient Rx LP | 2020-12-01 | HUMAN PRESCRIPTION DRUG LABEL | 3 |