TOPROL
- Product NDC
- 55154-9609
- 11-digit product format
- 551549609
- Labeler code
- 55154
- Product ID
- 55154-9609_89411e2c-2492-4cb4-87d4-8465f832d98b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol succinate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- NDA019962
- Marketing category
- NDA
- Marketing start
- 2010-05-10
- Marketing end
- 2019-10-31
- Substance
- METOPROLOL SUCCINATE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record