# Midodrine hydrochloride

NDC: 70771-1597
Generic name: Midodrine hydrochloride
Labeler / Manufacturer: Zydus Lifesciences Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20200917

FDA application: ANDA213055

## Active ingredients

- MIDODRINE HYDROCHLORIDE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70771-1597"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70771-1597
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b4c4417e-d8fd-46c8-b82f-ffbc8f201752