Package 50090-6179-1

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-6179-1
Digits Only 5009061791
Product NDC 50090-6179
Description

100 TABLET, FILM COATED in 1 BOTTLE (50090-6179-1)

Marketing

Marketing Status
Marketed Since 2022-10-20
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": "252c626f-1abb-4bd4-880b-504beb9ae6c7", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856783"], "spl_set_id": ["00d11130-c9ae-4258-9746-9763bc5deb84"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-6179-0)", "package_ndc": "50090-6179-0", "marketing_start_date": "20221020"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (50090-6179-1)", "package_ndc": "50090-6179-1", "marketing_start_date": "20221020"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-6179-6)", "package_ndc": "50090-6179-6", "marketing_start_date": "20221020"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-6179-7)", "package_ndc": "50090-6179-7", "marketing_start_date": "20231221"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "50090-6179_252c626f-1abb-4bd4-880b-504beb9ae6c7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "50090-6179", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA214548", "marketing_category": "ANDA", "marketing_start_date": "20210526", "listing_expiration_date": "20261231"}