Metoprolol succinate
- Product NDC
- 70518-1642
- 11-digit product format
- 705181642
- Labeler code
- 70518
- Product ID
- 70518-1642_96187765-b9b4-4126-e053-2995a90a89ba
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol succinate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA078889
- Marketing category
- ANDA
- Marketing start
- 2018-11-07
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record