# Mirtazapine

NDC: 63739-099
Generic name: Mirtazapine
Labeler / Manufacturer: McKesson Corporation dba SKY Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20070822
Marketing ended: 20270331
FDA application: ANDA077666

## Active ingredients

- MIRTAZAPINE: 30 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63739-099"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63739-099
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=40c95daa-bbd5-48d9-97e4-c87f2c1f0fa5