NDC 71335-3134 – Metoprolol succinate
Metoprolol Succinate 200 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC71335-3134
Product details
- Brand name
- Metoprolol succinate
- Generic name
- Metoprolol succinate
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA078889
- Marketed since
- September 10, 2012
- Listing expires
- December 31, 2027
- Pharmacologic class
- beta-Adrenergic Blocker
Active ingredients
- Metoprolol Succinate 200 mg/1
Uses, dosage, side effects and warnings for Metoprolol Succinate →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 71335-3134-1 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-3134-1) | May 21, 2026 |
| 71335-3134-2 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-3134-2) | May 21, 2026 |
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