# Zoloft

NDC: 0049-0050
Generic name: sertraline hydrochloride
Labeler / Manufacturer: ROERIG
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: SOLUTION, CONCENTRATE
Routes: ORAL
Marketing started: 20170106
Marketing ended: 20260630
FDA application: NDA020990

## Active ingredients

- SERTRALINE HYDROCHLORIDE: 20 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0049-0050"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0049-0050
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fe9e8b7d-61ea-409d-84aa-3ebd79a046b5