NDC 70436-167 – Metoprolol succinate
Metoprolol Succinate 200 mg/1 · Tablet, Extended Release · Oral
Product NDC70436-167
Product details
- Brand name
- Metoprolol succinate
- Generic name
- Metoprolol succinate
- Labeler
- Slate Run Pharmaceuticals, LLC
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA213854
- Marketed since
- April 29, 2021
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 70436-167-01 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-167-01) | Apr 29, 2021 |
| 70436-167-02 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-167-02) | Apr 29, 2021 |
| 70436-167-03 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-167-03) | Apr 29, 2021 |
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