# Midodrine Hydrochloride

NDC: 64980-433
Generic name: Midodrine Hydrochloride
Labeler / Manufacturer: Rising Pharma Holdings, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20190401

FDA application: ANDA207613

## 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:"64980-433"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=64980-433
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ffd4dfb9-a6d8-4c81-8b8c-8228d9e2f93e