# ESZOPICLONE

NDC: 47335-588
Generic name: ESZOPICLONE
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20140415

FDA application: ANDA091103

## Active ingredients

- ESZOPICLONE: 3 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"47335-588"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=47335-588
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8bb1965e-7845-4c5b-b021-38e251303d68