Package 70518-1612-1

Brand: trihexyphenidyl hydrochloride

Generic: trihexyphenidyl hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-1612-1
Digits Only 7051816121
Product NDC 70518-1612
Product ID 70518-1612_494f7eab-7c4c-b39f-e063-6294a90a71b3
Description

100 POUCH in 1 BOX (70518-1612-1) / 1 TABLET in 1 POUCH (70518-1612-2)

Marketing

Marketing Status
Marketed Since 2019-12-23
Brand trihexyphenidyl hydrochloride
Generic trihexyphenidyl hydrochloride
Sample Package No

Linked Drug Pages (1)

Trihexyphenidyl Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "494f7eab-7c4c-b39f-e063-6294a90a71b3", "openfda": {"unii": ["AO61G82577"], "rxcui": ["905269"], "spl_set_id": ["86a65e8a-10f4-4f12-8e65-2edf398daeaa"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-1612-1)  / 1 TABLET in 1 POUCH (70518-1612-2)", "package_ndc": "70518-1612-1", "marketing_start_date": "20191223"}], "brand_name": "Trihexyphenidyl Hydrochloride", "product_id": "70518-1612_494f7eab-7c4c-b39f-e063-6294a90a71b3", "dosage_form": "TABLET", "product_ndc": "70518-1612", "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": "ANDA084363", "marketing_category": "ANDA", "marketing_start_date": "20181029", "listing_expiration_date": "20271231"}