# Midodrine Hydrochloride

NDC: 72162-1973
Generic name: midodrine hydrochloride
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20201015

FDA application: ANDA207849

## Active ingredients

- MIDODRINE HYDROCHLORIDE: 2.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72162-1973"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72162-1973
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9c1ccd24-3f9c-489c-9fd2-98e69531d5ab