# Sertraline Hydrochloride

NDC: 65862-224
Generic name: Sertraline Hydrochloride
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION, CONCENTRATE
Routes: ORAL
Marketing started: 20081031

FDA application: ANDA078861

## Active ingredients

- SERTRALINE HYDROCHLORIDE: 20 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65862-224"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65862-224
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=01800452-c353-4235-a66a-214048752e74