# Clonidine Hydrochloride

NDC: 58657-649
Generic name: Clonidine Hydrochloride
Labeler / Manufacturer: Method Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20200701

FDA application: ANDA202297

## Active ingredients

- CLONIDINE HYDROCHLORIDE: .3 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"58657-649"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=58657-649
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=dffb5fdd-06c0-4275-9f89-9e12b3adf8a9