# Amitriptyline Hydrochloride

NDC: 69367-393
Generic name: Amitriptyline Hydrochloride
Labeler / Manufacturer: Westminster Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20240520

FDA application: ANDA212654

## Active ingredients

- AMITRIPTYLINE HYDROCHLORIDE: 150 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69367-393"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69367-393
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d46ff585-7082-4a7c-a88f-2acf3be0f1d5