NDC 68180-377 – Losartan Potassium
Losartan Potassium 50 mg/1 · Tablet · Oral
Product NDC68180-377
Product details
- Brand name
- Losartan Potassium
- Generic name
- Losartan Potassium
- Labeler
- Lupin Pharmaceuticals, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA078232
- Marketed since
- November 1, 2017
- 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 |
|---|---|---|
| 68180-377-03 | 1000 TABLET in 1 BOTTLE (68180-377-03) | Nov 1, 2017 |
| 68180-377-09 | 90 TABLET in 1 BOTTLE (68180-377-09) | Nov 1, 2017 |
Recalls mentioning this NDC
- D-0840-2022 May 11, 2022 · Class II
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits - D-0839-2022 May 11, 2022 · Class II
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits - D-0838-2022 May 11, 2022 · Class II
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
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