NDC 70518-3282 – Losartan Potassium
Losartan Potassium 50 mg/1 · Tablet · Oral
Product NDC70518-3282
Product details
- Brand name
- Losartan Potassium
- Generic name
- Losartan Potassium
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA078232
- Marketed since
- December 6, 2021
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 70518-3282-0 | 60 TABLET in 1 BLISTER PACK (70518-3282-0) | Dec 6, 2021 |
| 70518-3282-1 | 30 TABLET in 1 BLISTER PACK (70518-3282-1) | Dec 17, 2021 |
| 70518-3282-3 | 100 TABLET in 1 BOTTLE, PLASTIC (70518-3282-3) | Sep 17, 2026 |
Recalls mentioning this NDC
- D-0788-2022 May 4, 2022 · Class II
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits.
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