Package 67046-1625-3

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67046-1625-3
Digits Only 6704616253
Product NDC 67046-1625
Product ID 67046-1625_4616c30a-f8a2-6a3b-e063-6394a90a476e
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1625-3)

Marketing

Marketing Status
Marketed Since 2025-12-16
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": "4616c30a-f8a2-6a3b-e063-6394a90a476e", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856773"], "spl_set_id": ["4616c2be-03a5-4279-e063-6294a90ac052"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1625-3)", "package_ndc": "67046-1625-3", "marketing_start_date": "20251216"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "67046-1625_4616c30a-f8a2-6a3b-e063-6394a90a476e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "67046-1625", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA214548", "marketing_category": "ANDA", "marketing_start_date": "20251216", "listing_expiration_date": "20261231"}