# Clonidine Hydrochloride

NDC: 0143-9724
Generic name: Clonidine Hydrochloride
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20110101

FDA application: ANDA200300

## Active ingredients

- CLONIDINE HYDROCHLORIDE: 100 ug/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0143-9724"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0143-9724
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2a5b46ec-4c16-48a5-9e58-8d28a3f21274