NDC 43063-854 – Losartan Potassium
Losartan Potassium 50 mg/1 · Tablet, Film Coated · Oral
Product NDC43063-854
Product details
- Brand name
- Losartan Potassium
- Generic name
- Losartan Potassium
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA203835
- Marketed since
- August 19, 2015
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 43063-854-60 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-854-60) | Jan 14, 2019 |
| 43063-854-90 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-854-90) | May 29, 2018 |
Recalls mentioning this NDC
- D-0341-2021 May 5, 2021 · Class II
CGMP deviation: Product found to contain trace amounts of NMBA
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