NDC 68788-8639 – Losortan Potassium
Losartan Potassium 25 mg/1 · Tablet, Film Coated · Oral
Product NDC68788-8639
Product details
- Brand name
- Losortan Potassium
- Generic name
- Losartan Potassium
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078243
- Marketed since
- April 18, 2024
- Listing expires
- December 31, 2027
- Pharmacologic class
- Angiotensin 2 Receptor Blocker
Active ingredients
- Losartan Potassium 25 mg/1
Uses, dosage, side effects and warnings for Losortan Potassium →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 68788-8639-1 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-8639-1) | Apr 18, 2024 |
| 68788-8639-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-8639-3) | Apr 18, 2024 |
| 68788-8639-5 | 50 TABLET, FILM COATED in 1 BOTTLE (68788-8639-5) | Apr 18, 2024 |
| 68788-8639-6 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-8639-6) | Apr 18, 2024 |
| 68788-8639-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-8639-9) | Apr 18, 2024 |
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