TOPROL
- Product NDC
- 70518-1258
- 11-digit product format
- 705181258
- Labeler code
- 70518
- Product ID
- 70518-1258_9113d04e-cce8-4cc1-e053-2995a90a2e7b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol succinate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA019962
- Marketing category
- NDA
- Marketing start
- 2018-06-13
- Marketing end
- 0000-00-00
- Substance
- METOPROLOL SUCCINATE
- Active strength
- 50 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