# Midodrine Hydrochloride

NDC: 23155-970
Generic name: midodrine hydrochloride
Labeler / Manufacturer: Avet Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20260325

FDA application: ANDA076725

## 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:"23155-970"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=23155-970
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4d5e42be-3476-85d4-e063-6294a90a0865