# Metoprolol succinate

NDC: 75907-346
Generic name: Metoprolol succinate
Labeler / Manufacturer: Dr. Reddy's Laboratories Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20260113

FDA application: ANDA078889

## Active ingredients

- METOPROLOL SUCCINATE: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"75907-346"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=75907-346
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5b7095c8-f8b7-adc7-9052-92325da33a02