NDC 52817-361 – Metoprolol Tartrate
Metoprolol Tartrate 50 mg/1 · Tablet, Film Coated · Oral
Product NDC52817-361
Product details
- Brand name
- Metoprolol Tartrate
- Generic name
- Metoprolol Tartrate
- Labeler
- TruPharma LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA200981
- Marketed since
- December 1, 2018
- Listing expires
- December 31, 2026
- Pharmacologic class
- beta-Adrenergic Blocker
Active ingredients
- Metoprolol Tartrate 50 mg/1
Uses, dosage, side effects and warnings for Metoprolol Tartrate →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 52817-361-00 | 1000 TABLET, FILM COATED in 1 BOTTLE (52817-361-00) | Dec 1, 2018 |
| 52817-361-10 sample | 100 TABLET, FILM COATED in 1 BOTTLE (52817-361-10) | Dec 1, 2018 |
Recalls mentioning this NDC
- D-0517-2024 Jun 5, 2024 · Class II
Presence of Foreign Substance: metal in tablet - D-0362-2022 Jan 19, 2022 · Class II
Complaint received of foreign matter (metal) embedded in tablet.
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