Metoprolol Succinate
- Product NDC
- 55154-4385
- 11-digit product format
- 551544385
- Labeler code
- 55154
- Product ID
- 55154-4385_f9a52a3e-75cf-4131-a1ab-a4336e01ea5c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- metoprolol succinate
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA202033
- Marketing category
- ANDA
- Marketing start
- 2012-01-27
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record