Package 50268-041-15
Brand: amitriptyline hydrochloride
Generic: amitriptyline hydrochloridePackage Facts
Identity
Package NDC
50268-041-15
Digits Only
5026804115
Product NDC
50268-041
Description
50 BLISTER PACK in 1 BOX (50268-041-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-041-11)
Marketing
Marketing Status
Brand
amitriptyline hydrochloride
Generic
amitriptyline hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2b489726-9f79-c6d3-e063-6294a90a1ff3", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856762"], "spl_set_id": ["f5c5f3b6-e92b-1120-e053-2995a90ae8fa"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-041-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-041-11)", "package_ndc": "50268-041-15", "marketing_start_date": "20230228"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "50268-041_2b489726-9f79-c6d3-e063-6294a90a1ff3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "50268-041", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA214548", "marketing_category": "ANDA", "marketing_start_date": "20230228", "listing_expiration_date": "20261231"}