Package 50090-6927-0

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-6927-0
Digits Only 5009069270
Product NDC 50090-6927
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-6927-0)

Marketing

Marketing Status
Marketed Since 2023-12-14
Brand amitriptyline hydrochloride
Generic amitriptyline hydrochloride
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4e8ca436-5c2b-447f-8f9b-4aeae9e16da6", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856834"], "spl_set_id": ["5e8c8c5f-4964-4642-ad4b-69a75b2c8a02"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-6927-0)", "package_ndc": "50090-6927-0", "marketing_start_date": "20231214"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "50090-6927_4e8ca436-5c2b-447f-8f9b-4aeae9e16da6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "50090-6927", "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": "ANDA210086", "marketing_category": "ANDA", "marketing_start_date": "20210825", "listing_expiration_date": "20261231"}