# Amitriptyline Hydrochloride

NDC: 43063-822
Generic name: Amitriptyline Hydrochloride
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 19771121

FDA application: ANDA085968

## Active ingredients

- AMITRIPTYLINE HYDROCHLORIDE: 25 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43063-822"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43063-822
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1523a2b4-f9d6-4d3c-a370-df579ed36911