# Metoprolol Succinate

NDC: 68001-501
Generic name: Metoprolol Succinate ER Tablets
Labeler / Manufacturer: BluePoint Laboratories
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20210514

FDA application: ANDA211143

## Active ingredients

- METOPROLOL SUCCINATE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68001-501"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68001-501
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6588d77c-090f-4722-9c91-437887d4624a