NDC 65862-062 – Metoprolol Tartrate
Metoprolol Tartrate 25 mg/1 · Tablet, Film Coated · Oral
Product NDC65862-062
Product details
- Brand name
- Metoprolol Tartrate
- Generic name
- Metoprolol Tartrate
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077739
- Marketed since
- September 11, 2007
- Listing expires
- December 31, 2026
- Pharmacologic class
- beta-Adrenergic Blocker
Active ingredients
- Metoprolol Tartrate 25 mg/1
Uses, dosage, side effects and warnings for Metoprolol Tartrate →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 65862-062-01 | 100 TABLET, FILM COATED in 1 BOTTLE (65862-062-01) | Sep 11, 2007 |
| 65862-062-99 | 1000 TABLET, FILM COATED in 1 BOTTLE (65862-062-99) | Sep 11, 2007 |
Recalls mentioning this NDC
- D-0812-2021 Sep 29, 2021 · Class II
Presence of Foreign Substance: Product complaints received for the presence of metal wire in one tablet.
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