Metoprolol Tartrate
- Product NDC
- 82804-165
- 11-digit product format
- 828040165
- Labeler code
- 82804
- Product ID
- 82804-165_3c43fe89-2283-482e-9d97-648d3ed183f8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA200981
- Marketing category
- ANDA
- Marketing start
- 2018-12-01
- Substance
- METOPROLOL TARTRATE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| W5S57Y3A5L | METOPROLOL TARTRATE | 56392-17-7 | METOPROLOL TARTRATE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 82804-165-90 | 82804016590 | 90 TABLET, FILM COATED in 1 BOTTLE (82804-165-90) | 2024-12-16 | No | No | Historical |