# MIDODRINE HYDROCHLORIDE

NDC: 62332-339
Generic name: MIDODRINE HYDROCHLORIDE
Labeler / Manufacturer: Alembic Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20210122

FDA application: ANDA214734

## Active ingredients

- MIDODRINE HYDROCHLORIDE: 5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"62332-339"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62332-339
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=873c8e29-6961-4648-bfc8-f91c2086bd94