Package 70518-4048-1

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4048-1
Digits Only 7051840481
Product NDC 70518-4048
Description

30 TABLET in 1 BLISTER PACK (70518-4048-1)

Marketing

Marketing Status
Marketed Since 2024-04-10
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": "3fa0e65b-2ab0-3d3f-e063-6294a90af011", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856845"], "spl_set_id": ["5dc3c2d7-60a2-4754-be33-1f9401c925a4"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4048-1)", "package_ndc": "70518-4048-1", "marketing_start_date": "20240410"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (70518-4048-2)", "package_ndc": "70518-4048-2", "marketing_start_date": "20240904"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "70518-4048_3fa0e65b-2ab0-3d3f-e063-6294a90af011", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "70518-4048", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA217411", "marketing_category": "ANDA", "marketing_start_date": "20240410", "listing_expiration_date": "20261231"}