NDC 68788-7665 – Losartan Potassium
Losartan Potassium 50 mg/1 · Tablet, Film Coated · Oral
Product NDC68788-7665
Product details
- Brand name
- Losartan Potassium
- Generic name
- Losartan Potassium
- Labeler
- Preferred Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA203835
- Marketed since
- February 28, 2020
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 68788-7665-1 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-7665-1) | Feb 28, 2020 |
| 68788-7665-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-7665-3) | Feb 28, 2020 |
| 68788-7665-6 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-7665-6) | Feb 28, 2020 |
| 68788-7665-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-7665-9) | Feb 28, 2020 |
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