Package 50090-7513-0
Brand: amitriptyline hydrochloride
Generic: amitriptyline hydrochloridePackage Facts
Identity
Package NDC
50090-7513-0
Digits Only
5009075130
Product NDC
50090-7513
Description
90 TABLET, FILM COATED in 1 BOTTLE (50090-7513-0)
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": "2f8c7b57-4101-468c-b666-face4b0bcc4b", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856834"], "spl_set_id": ["bbbd535d-0bce-469e-917f-70a6ebd2f007"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7513-0)", "package_ndc": "50090-7513-0", "marketing_start_date": "20250224"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "50090-7513_2f8c7b57-4101-468c-b666-face4b0bcc4b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "50090-7513", "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": "25 mg/1"}], "application_number": "ANDA214548", "marketing_category": "ANDA", "marketing_start_date": "20210526", "listing_expiration_date": "20261231"}