NDC 75907-346 – Metoprolol succinate
Metoprolol Succinate 200 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC75907-346
Product details
- Brand name
- Metoprolol succinate
- Generic name
- Metoprolol succinate
- Labeler
- Dr. Reddy's Laboratories Inc
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA078889
- Marketed since
- January 13, 2026
- 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 |
|---|---|---|
| 75907-346-01 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (75907-346-01) | Jan 13, 2026 |
| 75907-346-05 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (75907-346-05) | Jan 13, 2026 |
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