NDC 60687-390 – Metoprolol Succinate
Metoprolol Succinate 25 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC60687-390
Product details
- Brand name
- Metoprolol Succinate
- Generic name
- Metoprolol Succinate
- Labeler
- American Health Packaging
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA090617
- Marketed since
- December 20, 2018
- Listing expires
- December 31, 2027
- Pharmacologic class
- beta-Adrenergic Blocker
Active ingredients
- Metoprolol Succinate 25 mg/1
Uses, dosage, side effects and warnings for Metoprolol Succinate →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 60687-390-01 | 100 BLISTER PACK in 1 CARTON (60687-390-01) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (60687-390-11) | Dec 20, 2018 |
| 60687-390-65 | 50 BLISTER PACK in 1 CARTON (60687-390-65) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (60687-390-11) | Mar 3, 2023 |
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