NDC 62332-116 – Metoprolol Tartrate and Hydrochlorothiazide
Metoprolol Tartrate 100 mg/1; Hydrochlorothiazide 25 mg/1 · Tablet · Oral
Product NDC62332-116
Product details
- Brand name
- Metoprolol Tartrate and Hydrochlorothiazide
- Generic name
- Metoprolol Tartrate and Hydrochlorothiazide
- Labeler
- Alembic Pharmaceuticals Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA202870
- Marketed since
- October 15, 2015
- Listing expires
- December 31, 2026
- Pharmacologic class
- Thiazide Diuretic; beta-Adrenergic Blocker
Active ingredients
- Metoprolol Tartrate 100 mg/1
- Hydrochlorothiazide 25 mg/1
Uses, dosage, side effects and warnings for Metoprolol Tartrate and Hydrochlorothiazide →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 62332-116-30 | 30 TABLET in 1 BOTTLE (62332-116-30) | Oct 15, 2015 |
| 62332-116-31 | 100 TABLET in 1 BOTTLE (62332-116-31) | Oct 15, 2015 |
| 62332-116-71 | 500 TABLET in 1 BOTTLE (62332-116-71) | Oct 15, 2015 |
Recalls mentioning this NDC
- D-0412-2021 Jun 2, 2021 · Class II
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
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