NDC 55111-467 – Metoprolol succinate
Metoprolol Succinate 50 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC55111-467
Product details
- Brand name
- Metoprolol succinate
- Generic name
- Metoprolol succinate
- Labeler
- Dr. Reddy's Laboratories Limited
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA090617
- Marketed since
- September 10, 2012
- 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 (5)
| Package NDC | Description | Since |
|---|---|---|
| 55111-467-01 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-467-01) | Sep 10, 2012 |
| 55111-467-05 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-467-05) | Sep 10, 2012 |
| 55111-467-30 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-467-30) | Sep 10, 2012 |
| 55111-467-60 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-467-60) | Sep 10, 2012 |
| 55111-467-78 | 10 BLISTER PACK in 1 CARTON (55111-467-78) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (55111-467-79) | Sep 10, 2012 |
Recalls mentioning this NDC
- D-1381-2014 Jun 18, 2014 · Class II
Failed Dissolution Specifications: Failure of dissolution test observed at the 18 month time point. - D-1080-2014 Feb 12, 2014 · Class II
Failed Dissolution Specification; 12-Month stability interval.
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