NDC 82868-084 – Metoprolol Succinate
Metoprolol Succinate 50 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC82868-084
Product details
- Brand name
- Metoprolol Succinate
- Generic name
- Metoprolol Succinate
- Labeler
- Northwind Health Company, LLC
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA216916
- Marketed since
- June 25, 2025
- Listing expires
- December 31, 2026
- Pharmacologic class
- beta-Adrenergic Blocker
Active ingredients
- Metoprolol Succinate 50 mg/1
Uses, dosage, side effects and warnings for Metoprolol Succinate →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 82868-084-30 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-084-30) | Aug 26, 2025 |
| 82868-084-90 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-084-90) | Jun 25, 2025 |
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