# Amitriptyline Hydrochloride

NDC: 29300-421
Generic name: Amitriptyline Hydrochloride
Labeler / Manufacturer: Unichem Pharmaceuticals (USA), Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20210526

FDA application: ANDA214548

## Active ingredients

- AMITRIPTYLINE HYDROCHLORIDE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"29300-421"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=29300-421
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9c6e0e05-b579-4fae-b768-e1a664c39bb8