NDC 71335-2083 – Losartan Potassium
Losartan Potassium 100 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-2083
Product details
- Brand name
- Losartan Potassium
- Generic name
- Losartan Potassium
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA091497
- Marketed since
- July 30, 2014
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin 2 Receptor Blocker
Active ingredients
- Losartan Potassium 100 mg/1
Uses, dosage, side effects and warnings for Losartan potassium →
Package NDC codes (8)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2083-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-2083-1) | Apr 14, 2023 |
| 71335-2083-2 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-2083-2) | Apr 14, 2023 |
| 71335-2083-3 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-2083-3) | Apr 14, 2023 |
| 71335-2083-4 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-2083-4) | Apr 14, 2023 |
| 71335-2083-5 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-2083-5) | Apr 14, 2023 |
| 71335-2083-6 | 28 TABLET, FILM COATED in 1 BOTTLE (71335-2083-6) | Apr 14, 2023 |
| 71335-2083-7 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-2083-7) | Apr 14, 2023 |
| 71335-2083-8 | 180 TABLET, FILM COATED in 1 BOTTLE (71335-2083-8) | Apr 14, 2023 |
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