Package 68071-3656-3

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-3656-3
Digits Only 6807136563
Product NDC 68071-3656
Product ID 68071-3656_1e78bc61-52f7-5a4c-e063-6394a90ab181
Description

30 TABLET in 1 BOTTLE (68071-3656-3)

Marketing

Marketing Status
Marketed Since 2024-07-30
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": "1e78bc61-52f7-5a4c-e063-6394a90ab181", "openfda": {"upc": ["0368071365634"], "unii": ["26LUD4JO9K"], "rxcui": ["856834"], "spl_set_id": ["1e78e304-00e8-7cb3-e063-6294a90a87ad"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3656-3)", "package_ndc": "68071-3656-3", "marketing_start_date": "20240730"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "68071-3656_1e78bc61-52f7-5a4c-e063-6394a90ab181", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "68071-3656", "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": "25 mg/1"}], "application_number": "ANDA217411", "marketing_category": "ANDA", "marketing_start_date": "20230610", "listing_expiration_date": "20261231"}