NDC 55111-469 – Metoprolol succinate
Metoprolol Succinate 200 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC55111-469
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 · ANDA078889
- Marketed since
- September 10, 2012
- 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 (5)
| Package NDC | Description | Since |
|---|---|---|
| 55111-469-01 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-469-01) | Sep 10, 2012 |
| 55111-469-05 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-469-05) | Sep 10, 2012 |
| 55111-469-30 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-469-30) | Sep 10, 2012 |
| 55111-469-60 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-469-60) | Sep 10, 2012 |
| 55111-469-78 | 10 BLISTER PACK in 1 CARTON (55111-469-78) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (55111-469-79) | Sep 10, 2012 |
Recalls mentioning this NDC
- D-0727-2018 May 16, 2018 · Class II
Presence of Foreign Tablets/Capsules: One foreign tablet identified as Clopidogrel 75 mg was found in a 100 count bottle of Metoprolol Succiante Extended-Release Tablets.
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