# SERTRALINE HYDROCHLORIDE

NDC: 43063-855
Generic name: SERTRALINE HYDROCHLORIDE
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
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:"43063-855"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43063-855
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=aa13261f-46a7-4381-8084-b3ad46221e2f