# Midodrine Hydrochloride

NDC: 0245-0212
Generic name: midodrine hydrochloride
Labeler / Manufacturer: Upsher-Smith laboratories, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20041103

FDA application: ANDA076725

## Active ingredients

- MIDODRINE HYDROCHLORIDE: 5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0245-0212"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0245-0212
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4c3517f3-1c68-4ade-b5f1-c488a3a335c1