# Clonidine Hydrochloride

NDC: 68180-606
Generic name: Clonidine Hydrochloride
Labeler / Manufacturer: Lupin Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20180207

FDA application: ANDA209285

## 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:"68180-606"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68180-606
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=745c8731-63e0-47ce-96d3-6a4d21c655e2