# Mirtazapine

NDC: 17856-0101
Generic name: Mirtazapine
Labeler / Manufacturer: ATLANTIC BIOLOGICALS CORP.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20090817

FDA application: ANDA076921

## Active ingredients

- MIRTAZAPINE: 7.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"17856-0101"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=17856-0101
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e6e5cbf7-a958-4ef8-abcc-a7491edb9520