Metoprolol Tartrate
- Product NDC
- 50090-4966
- 11-digit product format
- 500904966
- Labeler code
- 50090
- Product ID
- 50090-4966_052b2e4c-93c5-4c0d-b415-515159e2fa62
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077739
- Marketing category
- ANDA
- Marketing start
- 2007-09-11
- Marketing end
- 0000-00-00
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4966-0 | 50090496600 | 33 BLISTER PACK in 1 BOX, UNIT-DOSE (50090-4966-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 33 blister pack | 2020-03-16 | 0000-00-00 | No | No | Current |