Package 50268-040-15

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50268-040-15
Digits Only 5026804015
Product NDC 50268-040
Product ID 50268-040_2b489f9d-de0e-dd7a-e063-6394a90a8571
Description

50 BLISTER PACK in 1 BOX (50268-040-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-040-11)

Marketing

Marketing Status
Marketed Since 2023-06-06
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": "2b489f9d-de0e-dd7a-e063-6394a90a8571", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856783", "856834", "856845", "856853"], "spl_set_id": ["fd771b4b-c7ae-8e69-e053-6294a90a2120"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-040-15)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-040-11)", "package_ndc": "50268-040-15", "marketing_start_date": "20230606"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "50268-040_2b489f9d-de0e-dd7a-e063-6394a90a8571", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "50268-040", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA214548", "marketing_category": "ANDA", "marketing_start_date": "20230606", "listing_expiration_date": "20261231"}