NDC 71335-1221 – Losartan Potassium
Losartan Potassium 50 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-1221
Product details
- Brand name
- Losartan Potassium
- Generic name
- Losartan Potassium
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA090083
- Marketed since
- October 6, 2010
- 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 (8)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1221-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1221-1) | May 8, 2019 |
| 71335-1221-2 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1221-2) | May 22, 2019 |
| 71335-1221-3 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1221-3) | Jul 9, 2024 |
| 71335-1221-4 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-1221-4) | Jul 9, 2024 |
| 71335-1221-5 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-1221-5) | Sep 3, 2019 |
| 71335-1221-6 | 180 TABLET, FILM COATED in 1 BOTTLE (71335-1221-6) | Jul 9, 2024 |
| 71335-1221-7 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-1221-7) | Jul 9, 2024 |
| 71335-1221-8 | 7 TABLET, FILM COATED in 1 BOTTLE (71335-1221-8) | Jul 9, 2024 |
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