NDC 65862-203 – Losartan Potassium
Losartan Potassium 100 mg/1 · Tablet, Film Coated · Oral
Product NDC65862-203
Product details
- Brand name
- Losartan Potassium
- Generic name
- Losartan Potassium
- Labeler
- Aurobindo Pharma Limited
- 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 100 mg/1
Uses, dosage, side effects and warnings for Losartan potassium →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 65862-203-30 | 30 TABLET, FILM COATED in 1 BOTTLE (65862-203-30) | Oct 6, 2010 |
| 65862-203-90 | 90 TABLET, FILM COATED in 1 BOTTLE (65862-203-90) | Oct 6, 2010 |
| 65862-203-99 | 1000 TABLET, FILM COATED in 1 BOTTLE (65862-203-99) | Oct 6, 2010 |
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