# SERTRALINE HYDROCHLORIDE

NDC: 50090-7691
Generic name: sertraline hydrochloride
Labeler / Manufacturer: A-S Medication Solutions
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20210503

FDA application: ANDA214790

## 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:"50090-7691"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50090-7691
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2bb3a2d1-76c4-42e6-8553-aa95f263175b