Metoprolol Tartrate
- Product NDC
- 48433-313
- 11-digit product format
- 484330313
- Labeler code
- 48433
- Product ID
- 48433-313_238f1478-5514-495f-91c9-b3c7b9568a80
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol tartrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Safecor Health, LLC
- Application
- ANDA076670
- Marketing category
- ANDA
- Marketing start
- 2014-09-30
- Marketing end
- 0000-00-00
- Substance
- METOPROLOL TARTRATE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record