NDC 51655-519 – metoprolol succinate
Metoprolol Succinate 50 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC51655-519
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 · ANDA204161
- Marketed since
- December 19, 2022
- Listing expires
- December 31, 2027
- 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 |
|---|---|---|
| 51655-519-26 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-519-26) | Dec 19, 2022 |
| 51655-519-52 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-519-52) | Dec 19, 2022 |
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