Package 70518-2410-3

Brand: trihexyphenidyl hydrochloride

Generic: trihexyphenidyl hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-2410-3
Digits Only 7051824103
Product NDC 70518-2410
Description

100 POUCH in 1 BOX (70518-2410-3) / 1 TABLET in 1 POUCH (70518-2410-4)

Marketing

Marketing Status
Marketed Since 2021-07-16
Brand trihexyphenidyl hydrochloride
Generic trihexyphenidyl hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4a181afe-f595-8c9f-e063-6394a90ad7b0", "openfda": {"unii": ["AO61G82577"], "rxcui": ["905269"], "spl_set_id": ["b60ef86c-b8b6-4530-baaf-d4671ce961af"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-2410-3)  / 1 TABLET in 1 POUCH (70518-2410-4)", "package_ndc": "70518-2410-3", "marketing_start_date": "20210716"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-2410-5)", "package_ndc": "70518-2410-5", "marketing_start_date": "20230510"}], "brand_name": "TRIHEXYPHENIDYL HYDROCHLORIDE", "product_id": "70518-2410_4a181afe-f595-8c9f-e063-6394a90ad7b0", "dosage_form": "TABLET", "product_ndc": "70518-2410", "generic_name": "TRIHEXYPHENIDYL HYDROCHLORIDE", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRIHEXYPHENIDYL HYDROCHLORIDE", "active_ingredients": [{"name": "TRIHEXYPHENIDYL HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA040254", "marketing_category": "ANDA", "marketing_start_date": "20191108", "listing_expiration_date": "20271231"}