# Amoxapine

NDC: 62135-700
Generic name: Amoxapine
Labeler / Manufacturer: Chartwell RX, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19910628

FDA application: ANDA072879

## Active ingredients

- AMOXAPINE: 25 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"62135-700"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62135-700
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=eed5e856-dd7b-4eaa-9dad-508f2bef9328