Metoprolol Tartrate
- Product NDC
- 71610-559
- 11-digit product format
- 716100559
- Labeler code
- 71610
- Product ID
- 71610-559_4b804930-cb3d-41eb-b76f-afaff44ba395
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- metoprolol tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA076704
- Marketing category
- ANDA
- Marketing start
- 2004-01-16
- Substance
- METOPROLOL TARTRATE
- Active strength
- 100 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 |
|---|
| 71610-559-53 | 71610055953 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-559-53) | 2021-05-20 | No | No | Historical |
| 71610-559-60 | 71610055960 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-559-60) | 2021-05-20 | No | No | Historical |
| 71610-559-80 | 71610055980 | 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-559-80) | 2021-05-20 | No | No | Historical |