# Midodrine Hydrochloride

NDC: 52817-324
Generic name: Midodrine Hydrochloride
Labeler / Manufacturer: TruPharma, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20190819

FDA application: ANDA212543

## Active ingredients

- MIDODRINE HYDROCHLORIDE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"52817-324"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=52817-324
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a88cd5b5-bdcb-4ef7-8b04-ee4603bcd621