NDC 71335-0262 – Losartan Potassium
Losartan Potassium 50 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-0262
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 50 mg/1
Uses, dosage, side effects and warnings for Losartan potassium →
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0262-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0262-1) | Apr 22, 2019 |
| 71335-0262-2 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0262-2) | Apr 3, 2019 |
| 71335-0262-3 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0262-3) | Jan 20, 2022 |
| 71335-0262-4 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-0262-4) | Jan 20, 2022 |
| 71335-0262-5 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-0262-5) | Jan 20, 2022 |
| 71335-0262-6 | 180 TABLET, FILM COATED in 1 BOTTLE (71335-0262-6) | Jan 20, 2022 |
| 71335-0262-7 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-0262-7) | Jan 20, 2022 |
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