Metoprolol Succinate
- Product NDC
- 70518-0655
- 11-digit product format
- 705180655
- Labeler code
- 70518
- Product ID
- 70518-0655_89ad8173-6da9-28d3-e053-2a95a90afe0e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Succinate
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA076862
- Marketing category
- ANDA
- Marketing start
- 2017-08-01
- 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