# Metoprolol Tartrate

NDC: 70882-133
Generic name: Metoprolol Tartrate
Labeler / Manufacturer: Cambridge Therapeutics Technologies, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20070911

FDA application: ANDA077739

## Active ingredients

- METOPROLOL TARTRATE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70882-133"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70882-133
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e3a6e812-98ef-49bd-8319-c8fb9f46be06