NDC 68071-4755 – Metoprolol Tartrate
Metoprolol Tartrate 50 mg/1 · Tablet, Film Coated · Oral
Product NDC68071-4755
Product details
- Brand name
- Metoprolol Tartrate
- Generic name
- Metoprolol Tartrate
- Labeler
- NuCare Pharmaceuticals,Inc.
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 68071-4755-2 | 120 TABLET, FILM COATED in 1 BOTTLE (68071-4755-2) | Feb 6, 2019 |
| 68071-4755-8 | 180 TABLET, FILM COATED in 1 BOTTLE (68071-4755-8) | Feb 6, 2019 |
| 68071-4755-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68071-4755-9) | Feb 6, 2019 |
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