Package 60687-444-01

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60687-444-01
Digits Only 6068744401
Product NDC 60687-444
Description

100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-444-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-444-11)

Marketing

Marketing Status
Marketed Since 2019-08-12
Brand amitriptyline hydrochloride
Generic amitriptyline hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "44706732-5523-8018-e063-6294a90a9cc7", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856834", "856845"], "spl_set_id": ["98cc0bf3-ae5b-47cc-992f-9157fed7c3f4"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-444-01)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-444-11)", "package_ndc": "60687-444-01", "marketing_start_date": "20190812"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "60687-444_44706732-5523-8018-e063-6294a90a9cc7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "60687-444", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA210086", "marketing_category": "ANDA", "marketing_start_date": "20190812", "listing_expiration_date": "20261231"}