# SERTRALINE

NDC: 76282-213
Generic name: Sertraline
Labeler / Manufacturer: Exelan Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20120820

FDA application: ANDA077397

## Active ingredients

- SERTRALINE HYDROCHLORIDE: 50 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"76282-213"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76282-213
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2dac437f-b5ef-42dd-aa0b-1f4b9b45ef43