Metoprolol Tartrate And Hydrochlorothiazide 62756-0368
Product NDC
62756-0368- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 1, 2022
- Listing Expires
- December 31, 2026
- Application
- ANDA090654
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydrochlorothiazide | 25 mg/1 |
| Metoprolol Tartrate | 100 mg/1 |
Drug Class
Thiazide Diuretic [EPC]Adrenergic beta-Antagonists [MoA]Increased Diuresis [PE]
Packaging Options(4)
100 TABLET in 1 BOTTLE (62756-368-08)
1000 TABLET in 1 BOTTLE (62756-368-18)
30 TABLET in 1 BOTTLE (62756-368-83)
100 TABLET in 1 BOTTLE (62756-368-88)