Losartan Potassium
- Product NDC
- 57237-205
- 11-digit product format
- 572370205
- Labeler code
- 57237
- Product ID
- 57237-205_ff1828e1-ee17-4b2c-a687-8390d891ce75
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Rising Health, LLC
- Application
- ANDA090083
- Marketing category
- ANDA
- Marketing start
- 2010-10-06
- Marketing end
- 0000-00-00
- Substance
- LOSARTAN POTASSIUM
- Active strength
- 50 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 57237-205-30 | 57237020530 | 30 TABLET, FILM COATED in 1 BOTTLE (57237-205-30) | 2010-10-06 | 0000-00-00 | No | No | Current |
| 57237-205-90 | 57237020590 | 90 TABLET, FILM COATED in 1 BOTTLE (57237-205-90) | 2010-10-06 | 0000-00-00 | No | No | Current |
| 57237-205-99 | 57237020599 | 1000 TABLET, FILM COATED in 1 BOTTLE (57237-205-99) | 2010-10-06 | 0000-00-00 | No | No | Current |