NDC 71205-281 – Losartan Potassium
Losartan Potassium 50 mg/1 · Tablet, Film Coated · Oral
Product NDC71205-281
Product details
- Brand name
- Losartan Potassium
- Generic name
- Losartan Potassium
- Labeler
- Proficient Rx LP
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 71205-281-30 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-281-30) | Jun 1, 2019 |
| 71205-281-60 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-281-60) | Jun 1, 2019 |
| 71205-281-90 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-281-90) | Jun 1, 2019 |
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