Package 69367-392-01

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69367-392-01
Digits Only 6936739201
Product NDC 69367-392
Product ID 69367-392_3991983c-6f46-46e2-825c-ed9e5d4c1cb4
Description

100 TABLET, COATED in 1 BOTTLE (69367-392-01)

Marketing

Marketing Status
Marketed Since 2024-05-20
Brand amitriptyline hydrochloride
Generic amitriptyline hydrochloride
Sample Package No

Linked Drug Pages (1)

Amitriptyline Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3991983c-6f46-46e2-825c-ed9e5d4c1cb4", "openfda": {"upc": ["0369367391016", "0369367393010", "0369367392013", "0369367388016", "0369367390019", "0369367389013"], "unii": ["26LUD4JO9K"], "rxcui": ["856762", "856773", "856783", "856834", "856845", "856853"], "spl_set_id": ["d46ff585-7082-4a7c-a88f-2acf3be0f1d5"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (69367-392-01)", "package_ndc": "69367-392-01", "marketing_start_date": "20240520"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "69367-392_3991983c-6f46-46e2-825c-ed9e5d4c1cb4", "dosage_form": "TABLET, COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "69367-392", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA212654", "marketing_category": "ANDA", "marketing_start_date": "20240520", "listing_expiration_date": "20261231"}