NDC 71335-0167 – Metoprolol succinate
Metoprolol Succinate 100 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC71335-0167
Product details
- Brand name
- Metoprolol succinate
- Generic name
- Metoprolol succinate
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA078889
- Marketed since
- September 10, 2012
- Listing expires
- December 31, 2026
- Pharmacologic class
- beta-Adrenergic Blocker
Active ingredients
- Metoprolol Succinate 100 mg/1
Uses, dosage, side effects and warnings for Metoprolol Succinate →
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0167-1 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0167-1) | Feb 12, 2018 |
| 71335-0167-2 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0167-2) | Feb 16, 2018 |
| 71335-0167-3 | 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0167-3) | Feb 14, 2018 |
| 71335-0167-4 | 20 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0167-4) | May 2, 2022 |
| 71335-0167-5 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0167-5) | May 2, 2022 |
| 71335-0167-6 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0167-6) | May 2, 2022 |
| 71335-0167-7 | 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0167-7) | May 2, 2022 |
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