Package 68788-8218-6

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68788-8218-6
Digits Only 6878882186
Product NDC 68788-8218
Description

60 TABLET, FILM COATED in 1 BOTTLE (68788-8218-6)

Marketing

Marketing Status
Marketed Since 2022-09-08
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": "82d00754-2c99-43ed-af8b-7cfa29e8df32", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856783"], "spl_set_id": ["5dd07852-43a5-415c-863e-1202f82b5654"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-8218-3)", "package_ndc": "68788-8218-3", "marketing_start_date": "20220908"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-8218-6)", "package_ndc": "68788-8218-6", "marketing_start_date": "20220908"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-8218-9)", "package_ndc": "68788-8218-9", "marketing_start_date": "20220908"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "68788-8218_82d00754-2c99-43ed-af8b-7cfa29e8df32", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "68788-8218", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "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": "20220908", "listing_expiration_date": "20271231"}