NDC 68180-215 – Losartan Potassium and Hydrochlorothiazide
Hydrochlorothiazide 12.5 mg/1; Losartan Potassium 50 mg/1 · Tablet · Oral
Product NDC68180-215
Product details
- Brand name
- Losartan Potassium and Hydrochlorothiazide
- Generic name
- Losartan Potassium and Hydrochlorothiazide
- Labeler
- Lupin Pharmaceuticals, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA078245
- Marketed since
- October 6, 2010
- Listing expires
- December 31, 2027
- Pharmacologic class
- Angiotensin 2 Receptor Blocker; Thiazide Diuretic
Active ingredients
- Hydrochlorothiazide 12.5 mg/1
- Losartan Potassium 50 mg/1
Uses, dosage, side effects and warnings for Losartan Potassium and Hydrochlorothiazide →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 68180-215-06 | 30 TABLET in 1 BOTTLE (68180-215-06) | Oct 6, 2010 |
| 68180-215-09 | 90 TABLET in 1 BOTTLE (68180-215-09) | Oct 6, 2010 |
Recalls mentioning this NDC
- D-0841-2022 May 11, 2022 · Class II
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits - D-0843-2022 May 11, 2022 · Class II
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits - D-0842-2022 May 11, 2022 · Class II
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
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