NDC 70771-1341 – Metoprolol succinate
Metoprolol Succinate 200 mg/1 · Tablet, Extended Release · Oral
Product NDC70771-1341
Product details
- Brand name
- Metoprolol succinate
- Generic name
- Metoprolol succinate
- Labeler
- Zydus Lifesciences Limited
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA203894
- Marketed since
- June 7, 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 70771-1341-0 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1341-0) | Jun 7, 2018 |
| 70771-1341-1 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1341-1) | Jun 7, 2018 |
| 70771-1341-5 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1341-5) | Jun 7, 2018 |
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