# METOPROLOL TARTRATE AND HYDROCHLOROTHIAZIDE

NDC: 27241-301
Generic name: metoprolol tartrate and hydrochlorothiazide
Labeler / Manufacturer: Ajanta Pharma USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250315

FDA application: ANDA215789

## Active ingredients

- HYDROCHLOROTHIAZIDE: 25 mg/1
- METOPROLOL TARTRATE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"27241-301"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=27241-301
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8b78d7ad-22a8-4a9f-afb5-d18f0a4e6d36