# Midodrine Hydrochloride

NDC: 49884-814
Generic name: Midodrine Hydrochloride
Labeler / Manufacturer: Endo USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20181029

FDA application: ANDA207169

## 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:"49884-814"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=49884-814
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=863f12bd-d4a9-4547-8667-5dfa9e2ce6d1