Metoprolol Succinate
- Product NDC
- 50436-7056
- 11-digit product format
- 504367056
- Labeler code
- 50436
- Product ID
- 50436-7056_f8c5fb16-a7df-440b-aeaf-f17971ffb6e6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Succinate
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA090615
- Marketing category
- ANDA
- Marketing start
- 2010-07-22
- Marketing end
- 0000-00-00
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record