NDC 71335-1102 – Losartan Potassium
Losartan Potassium 50 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-1102
Product details
- Brand name
- Losartan Potassium
- Generic name
- Losartan Potassium
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA203835
- Marketed since
- August 19, 2015
- 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 (8)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1102-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1102-1) | Mar 16, 2016 |
| 71335-1102-2 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1102-2) | Mar 16, 2016 |
| 71335-1102-3 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1102-3) | Mar 16, 2016 |
| 71335-1102-4 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-1102-4) | Mar 16, 2016 |
| 71335-1102-5 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-1102-5) | Mar 16, 2016 |
| 71335-1102-6 | 180 TABLET, FILM COATED in 1 BOTTLE (71335-1102-6) | Mar 16, 2016 |
| 71335-1102-7 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-1102-7) | Mar 16, 2016 |
| 71335-1102-8 | 7 TABLET, FILM COATED in 1 BOTTLE (71335-1102-8) | Mar 16, 2016 |
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