NDC 46708-446 – Losartan Potassium
Losartan Potassium 50 mg/1 · Tablet, Film Coated · Oral
Product NDC46708-446
Product details
- Brand name
- Losartan Potassium
- Generic name
- Losartan Potassium
- Labeler
- Alembic Pharmaceuticals Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA090428
- Marketed since
- May 23, 2016
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 46708-446-30 | 30 TABLET, FILM COATED in 1 BOTTLE (46708-446-30) | May 23, 2016 |
| 46708-446-31 | 100 TABLET, FILM COATED in 1 BOTTLE (46708-446-31) | May 23, 2016 |
| 46708-446-90 | 90 TABLET, FILM COATED in 1 BOTTLE (46708-446-90) | May 23, 2016 |
| 46708-446-91 | 1000 TABLET, FILM COATED in 1 BOTTLE (46708-446-91) | May 23, 2016 |
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