# Clonidine Hydrochloride

NDC: 0904-7442
Generic name: clonidine hydrochloride
Labeler / Manufacturer: Major Pharmaceuticals
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20240731

FDA application: ANDA077901

## 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:"0904-7442"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0904-7442
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8171776a-dd14-4dcc-8860-3c27d8ea9504