# Midodrine Hydrochloride

NDC: 59651-246
Generic name: Midodrine Hydrochloride
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20200810

FDA application: ANDA212774

## 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:"59651-246"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59651-246
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=771b3e81-f15b-4d32-a1d8-c43b104d1f7b