# Amitriptyline Hydrochloride

NDC: 57664-689
Generic name: Amitriptyline Hydrochloride
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 19870714

FDA application: ANDA089399

## 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:"57664-689"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=57664-689
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4e520c63-1cf6-40f6-a51c-3f9b0e181342