Package 70710-1226-0

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70710-1226-0
Digits Only 7071012260
Product NDC 70710-1226
Product ID 70710-1226_5160111f-8889-4057-aa2a-519eccd14a5e
Description

1000 TABLET, FILM COATED in 1 BOTTLE (70710-1226-0)

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": "5160111f-8889-4057-aa2a-519eccd14a5e", "openfda": {"upc": ["0370710122911", "0370710122713"], "unii": ["26LUD4JO9K"], "rxcui": ["856762", "856773", "856783", "856834", "856845", "856853"], "spl_set_id": ["73669354-babc-4687-a4fe-ad0fc1f863ba"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (70710-1226-0)", "package_ndc": "70710-1226-0", "marketing_start_date": "20171226"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (70710-1226-1)", "package_ndc": "70710-1226-1", "marketing_start_date": "20171226"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "70710-1226_5160111f-8889-4057-aa2a-519eccd14a5e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "70710-1226", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "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": "20171226", "listing_expiration_date": "20261231"}