NDC 65841-731 – Losartan Potassium
Losartan Potassium 100 mg/1 · Tablet, Film Coated · Oral
Product NDC65841-731
Product details
- Brand name
- Losartan Potassium
- Generic name
- Losartan Potassium
- Labeler
- Zydus Lifesciences Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078243
- Marketed since
- October 4, 2010
- Listing expires
- December 31, 2027
- 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 (5)
| Package NDC | Description | Since |
|---|---|---|
| 65841-731-01 | 100 TABLET, FILM COATED in 1 BOTTLE (65841-731-01) | Oct 4, 2010 |
| 65841-731-06 | 30 TABLET, FILM COATED in 1 BOTTLE (65841-731-06) | Oct 4, 2010 |
| 65841-731-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (65841-731-10) | Oct 4, 2010 |
| 65841-731-16 | 90 TABLET, FILM COATED in 1 BOTTLE (65841-731-16) | Oct 4, 2010 |
| 65841-731-77 | 10 BLISTER PACK in 1 CARTON (65841-731-77) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65841-731-30) | Oct 4, 2010 |
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