Package 68071-3913-3

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-3913-3
Digits Only 6807139133
Product NDC 68071-3913
Product ID 68071-3913_434543c0-554b-65ca-e063-6394a90a7bd5
Description

30 TABLET, FILM COATED in 1 BOTTLE (68071-3913-3)

Marketing

Marketing Status
Marketed Since 2025-11-10
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": "434543c0-554b-65ca-e063-6394a90a7bd5", "openfda": {"upc": ["0368071391336"], "unii": ["26LUD4JO9K"], "rxcui": ["856783"], "spl_set_id": ["43454445-b9cf-1378-e063-6294a90a1cc6"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-3913-3)", "package_ndc": "68071-3913-3", "marketing_start_date": "20251110"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "68071-3913_434543c0-554b-65ca-e063-6394a90a7bd5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "68071-3913", "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": "ANDA210086", "marketing_category": "ANDA", "marketing_start_date": "20210825", "listing_expiration_date": "20261231"}