# Clonidine

NDC: 39822-2000
Generic name: Clonidine
Labeler / Manufacturer: XGen Pharmaceuticals DJB, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: EPIDURAL
Marketing started: 20131029

FDA application: ANDA203167

## Active ingredients

- CLONIDINE HYDROCHLORIDE: 100 ug/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"39822-2000"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=39822-2000
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ada02f1f-ae78-4435-879e-492ae862d504