# Sertraline Hydrochloride

NDC: 16714-613
Generic name: Sertraline Hydrochloride
Labeler / Manufacturer: NorthStar Rx LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20070206

FDA application: ANDA077206

## Active ingredients

- SERTRALINE HYDROCHLORIDE: 100 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"16714-613"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16714-613
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9bc362d4-489c-4e7f-915a-3076ff8d132a