Metoprolol Succinate 82868-0084
Product NDC
82868-0084- Manufacturer
- Northwind Health Company, Llc
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 25, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA216916
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Metoprolol Succinate | 50 mg/1 |
Drug Class
Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]
Packaging Options(2)
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-084-30)
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-084-90)