Package 70518-2409-2
Brand: trihexyphenidyl hydrochloride
Generic: trihexyphenidyl hydrochloridePackage Facts
Identity
Package NDC
70518-2409-2
Digits Only
7051824092
Product NDC
70518-2409
Description
100 POUCH in 1 BOX (70518-2409-2) / 1 TABLET in 1 POUCH (70518-2409-3)
Marketing
Marketing Status
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": "4a17b684-8b80-215c-e063-6394a90a6e19", "openfda": {"unii": ["AO61G82577"], "rxcui": ["905283"], "spl_set_id": ["c25ea809-5bdf-4917-97f1-610059fbd0b7"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-2409-2) / 1 TABLET in 1 POUCH (70518-2409-3)", "package_ndc": "70518-2409-2", "marketing_start_date": "20210511"}], "brand_name": "TRIHEXYPHENIDYL HYDROCHLORIDE", "product_id": "70518-2409_4a17b684-8b80-215c-e063-6394a90a6e19", "dosage_form": "TABLET", "product_ndc": "70518-2409", "generic_name": "TRIHEXYPHENIDYL HYDROCHLORIDE", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRIHEXYPHENIDYL HYDROCHLORIDE", "active_ingredients": [{"name": "TRIHEXYPHENIDYL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA040254", "marketing_category": "ANDA", "marketing_start_date": "20191108", "listing_expiration_date": "20271231"}