Package 16571-106-10
Brand: amitriptyline hydrochloride
Generic: amitriptyline hydrochloridePackage Facts
Identity
Package NDC
16571-106-10
Digits Only
1657110610
Product NDC
16571-106
Description
1000 TABLET in 1 BOTTLE (16571-106-10)
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": "a83b8840-dd78-46f1-b952-893c30bf5bf9", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856762", "856773", "856783", "856834", "856845", "856853"], "spl_set_id": ["a219a68e-7ce5-4e9d-a0de-ec76960040f6"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (16571-106-01)", "package_ndc": "16571-106-01", "marketing_start_date": "20230610"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (16571-106-10)", "package_ndc": "16571-106-10", "marketing_start_date": "20230610"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "16571-106_a83b8840-dd78-46f1-b952-893c30bf5bf9", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "16571-106", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA217411", "marketing_category": "ANDA", "marketing_start_date": "20230610", "listing_expiration_date": "20261231"}