Metoprolol Tartrate
- Product NDC
- 50436-6578
- 11-digit product format
- 504366578
- Labeler code
- 50436
- Product ID
- 50436-6578_99fd3e64-2723-4ba6-a435-595239e2d2db
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA078459
- Marketing category
- ANDA
- Marketing start
- 2009-03-15
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record