Metoprolol Tartrate
- Product NDC
- 60760-524
- 11-digit product format
- 607600524
- Labeler code
- 60760
- Product ID
- 60760-524_2b499846-132e-a669-e063-6394a90a59fb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- ST. MARY'S MEDICAL PARK PHARMACY
- 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 |
|---|
| 60760-524-60 | 60760052460 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-524-60) | 2022-08-30 | No | No | Historical |
| 60760-524-98 | 60760052498 | 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-524-98) | 2022-06-17 | No | No | Historical |