# Clonidine hydrochloride

NDC: 60687-462
Generic name: Clonidine hydrochloride
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20191217

FDA application: ANDA209686

## Active ingredients

- CLONIDINE HYDROCHLORIDE: .1 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60687-462"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60687-462
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=95b390cc-0578-4cb0-9c08-4853388b2ec9