Package 63850-0022-2

Brand: trihexyphenidyl hydrochloride

Generic: trihexyphenidyl hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63850-0022-2
Digits Only 6385000222
Product NDC 63850-0022
Product ID 63850-0022_2b77cfd6-ad8a-4cbf-a22c-eb69e7a8548c
Description

1000 TABLET in 1 BOTTLE (63850-0022-2)

Marketing

Marketing Status
Marketed Since 2010-10-17
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": "2b77cfd6-ad8a-4cbf-a22c-eb69e7a8548c", "openfda": {"upc": ["0363850002113", "0363850002229"], "unii": ["AO61G82577"], "rxcui": ["905269", "905283"], "spl_set_id": ["b7e4200c-feff-4537-aad1-cf9989fd8c14"], "manufacturer_name": ["Natco Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (63850-0022-1)", "package_ndc": "63850-0022-1", "marketing_start_date": "20101017"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (63850-0022-2)", "package_ndc": "63850-0022-2", "marketing_start_date": "20101017"}], "brand_name": "Trihexyphenidyl Hydrochloride", "product_id": "63850-0022_2b77cfd6-ad8a-4cbf-a22c-eb69e7a8548c", "dosage_form": "TABLET", "product_ndc": "63850-0022", "generic_name": "Trihexyphenidyl Hydrochloride", "labeler_name": "Natco Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trihexyphenidyl Hydrochloride", "active_ingredients": [{"name": "TRIHEXYPHENIDYL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA091630", "marketing_category": "ANDA", "marketing_start_date": "20101007", "listing_expiration_date": "20261231"}