# Metoprolol Tartrate and Hydrochlorothiazide

NDC: 0378-0434
Generic name: metoprolol tartrate and hydrochlorothiazide
Labeler / Manufacturer: Mylan Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20040820

FDA application: ANDA076792

## Active ingredients

- HYDROCHLOROTHIAZIDE: 25 mg/1
- METOPROLOL TARTRATE: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0378-0434"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0378-0434
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b6cf0f43-8dc3-4535-b651-daf1f9e0336c