Metoprolol Succinate 55111-0469
Product NDC
55111-0469- Manufacturer
- Dr. Reddy's Laboratories Limited
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 10, 2012
- Listing Expires
- December 31, 2026
- Application
- ANDA078889
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Metoprolol Succinate | 200 mg/1 |
Drug Class
Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]
Packaging Options(5)
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-469-01)
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-469-05)
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-469-30)
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-469-60)
10 BLISTER PACK in 1 CARTON (55111-469-78) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (55111-469-79)