Package 68071-4104-1

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-4104-1
Digits Only 6807141041
Product NDC 68071-4104
Product ID 68071-4104_1d8e3ff7-d1f4-0a8a-e063-6294a90ac4ae
Description

100 TABLET, FILM COATED in 1 BOTTLE (68071-4104-1)

Marketing

Marketing Status
Marketed Since 2017-09-29
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": "1d8e3ff7-d1f4-0a8a-e063-6294a90ac4ae", "openfda": {"upc": ["0368071410419"], "unii": ["26LUD4JO9K"], "rxcui": ["856783"], "spl_set_id": ["5a5a4040-5395-54ac-e053-2991aa0aa4ab"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68071-4104-1)", "package_ndc": "68071-4104-1", "marketing_start_date": "20170929"}], "brand_name": "AMITRIPTYLINE HYDROCHLORIDE", "product_id": "68071-4104_1d8e3ff7-d1f4-0a8a-e063-6294a90ac4ae", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "68071-4104", "generic_name": "AMITRIPTYLINE HYDROCHLORIDE", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AMITRIPTYLINE HYDROCHLORIDE", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA202446", "marketing_category": "ANDA", "marketing_start_date": "20141205", "listing_expiration_date": "20261231"}