NDC 64380-934 – LOSARTAN POTASSIUM 50 mg
Losartan Potassium 50 mg/1 · Tablet, Film Coated · Oral
Product NDC64380-934
Product details
- Brand name
- LOSARTAN POTASSIUM 50 mg
- Generic name
- Losartan Potassium
- Labeler
- Strides Pharma Science Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA090382
- Marketed since
- October 9, 2019
- 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 |
|---|---|---|
| 64380-934-04 | 30 TABLET, FILM COATED in 1 BOTTLE (64380-934-04) | Oct 9, 2019 |
| 64380-934-05 | 90 TABLET, FILM COATED in 1 BOTTLE (64380-934-05) | Oct 9, 2019 |
| 64380-934-08 | 1000 TABLET, FILM COATED in 1 BOTTLE (64380-934-08) | Oct 9, 2019 |
Recalls mentioning this NDC
- D-0895-2023 Jul 12, 2023 · Class II
Presence of Foreign Substance: Presence of a small piece of blue plastic embedded in the tablet. - D-0973-2022 Jun 8, 2022 · Class II
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits - D-0972-2022 Jun 8, 2022 · Class II
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits - D-0974-2022 Jun 8, 2022 · Class II
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
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