NDC 50742-618 – Metoprolol Succinate
Metoprolol Succinate 200 mg/1 · Tablet, Extended Release · Oral
Product NDC50742-618
Product details
- Brand name
- Metoprolol Succinate
- Generic name
- Metoprolol succinate
- Labeler
- Ingenus Pharmaceuticals, LLC
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA204106
- Marketed since
- February 6, 2018
- 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 (5)
| Package NDC | Description | Since |
|---|---|---|
| 50742-618-01 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-618-01) | Feb 6, 2018 |
| 50742-618-05 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-618-05) | Feb 6, 2018 |
| 50742-618-10 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-618-10) | Feb 6, 2018 |
| 50742-618-90 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-618-90) | Feb 6, 2018 |
| 50742-618-99 | 16181 TABLET, EXTENDED RELEASE in 1 DRUM (50742-618-99) | Apr 9, 2021 |
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