# Droxidopa

NDC: 67877-705
Generic name: Droxidopa
Labeler / Manufacturer: Ascend Laboratories, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20210219

FDA application: ANDA213911

## Active ingredients

- DROXIDOPA: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"67877-705"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67877-705
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6091958e-f04e-47c0-9eef-9c204df4edd9