Metoprolol Succinate
- Product NDC
- 68788-6785
- 11-digit product format
- 687886785
- Labeler code
- 68788
- Product ID
- 68788-6785_bf3907fc-a2fa-4e55-9e7f-c5b3af81094b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Succinate
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA077298
- Marketing category
- ANDA
- Marketing start
- 2016-11-02
- 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