NDC 51655-795 – Losartan Potassium
Losartan Potassium 50 mg/1 · Tablet, Film Coated · Oral
Product NDC51655-795
Product details
- Brand name
- Losartan Potassium
- Generic name
- Losartan Potassium
- Labeler
- Northwind Health Company, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA090083
- Marketed since
- January 19, 2022
- Listing expires
- December 31, 2027
- Pharmacologic class
- Angiotensin 2 Receptor Blocker
Active ingredients
- Losartan Potassium 50 mg/1
Uses, dosage, side effects and warnings for Losartan potassium →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 51655-795-26 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-795-26) | Jan 19, 2022 |
| 51655-795-52 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-795-52) | Jan 20, 2022 |
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