# Clonidine

NDC: 50742-247
Generic name: clonidine
Labeler / Manufacturer: Ingenus Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20190305

FDA application: ANDA209675

## 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:"50742-247"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50742-247
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=99485427-a120-4fc7-bb61-25857d1900ec