# SERTRALINE HYDROCHLORIDE

NDC: 71205-028
Generic name: SERTRALINE HYDROCHLORIDE
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20170209

FDA application: ANDA202825

## Active ingredients

- SERTRALINE HYDROCHLORIDE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71205-028"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71205-028
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6b532e6a-b040-4a10-a242-fb6d8dfc0852