Metoprolol Tartrate
- Product NDC
- 50090-1563
- 11-digit product format
- 500901563
- Labeler code
- 50090
- Product ID
- 50090-1563_28b6e2ad-acc7-4422-be93-421d78ad9b69
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- metoprolol tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076704
- Marketing category
- ANDA
- Marketing start
- 1993-12-23
- Marketing end
- 0000-00-00
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record