Package 70771-1173-1

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70771-1173-1
Digits Only 7077111731
Product NDC 70771-1173
Product ID 70771-1173_64a2af6e-d243-4263-96f3-4c2b3707bf11
Description

100 TABLET, FILM COATED in 1 BOTTLE (70771-1173-1)

Marketing

Marketing Status
Marketed Since 2017-12-26
Brand amitriptyline hydrochloride
Generic amitriptyline hydrochloride
Sample Package No

Linked Drug Pages (1)

Amitriptyline Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "64a2af6e-d243-4263-96f3-4c2b3707bf11", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856762", "856773", "856783", "856834", "856845", "856853"], "spl_set_id": ["4159b10e-f589-486c-969d-9b4544b098b5"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (70771-1173-0)", "package_ndc": "70771-1173-0", "marketing_start_date": "20171226"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (70771-1173-1)", "package_ndc": "70771-1173-1", "marketing_start_date": "20171226"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "70771-1173_64a2af6e-d243-4263-96f3-4c2b3707bf11", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "70771-1173", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA210086", "marketing_category": "ANDA", "marketing_start_date": "20171226", "listing_expiration_date": "20261231"}