# Sertraline hydrochloride

NDC: 70010-203
Generic name: Sertraline hydrochloride
Labeler / Manufacturer: Granules Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20230515

FDA application: ANDA078403

## Active ingredients

- SERTRALINE HYDROCHLORIDE: 25 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70010-203"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70010-203
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=98960cc1-1d44-4d89-b415-7e250cc762cc