NDC 72162-1859 – Metoprolol Succinate
Metoprolol Succinate 200 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC72162-1859
Product details
- Brand name
- Metoprolol Succinate
- Generic name
- Metoprolol Succinate ER Tablets
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA211143
- Marketed since
- November 27, 2020
- Listing expires
- December 31, 2026
- Pharmacologic class
- beta-Adrenergic Blocker
Active ingredients
- Metoprolol Succinate 200 mg/1
Uses, dosage, side effects and warnings for Metoprolol Succinate →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 72162-1859-0 | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1859-0) | Jul 16, 2024 |
| 72162-1859-1 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1859-1) | Mar 7, 2024 |
| 72162-1859-5 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1859-5) | Mar 7, 2024 |
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