Package 69452-242-20

Brand: trihexyphenidyl hydrochloride

Generic: trihexyphenidyl hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69452-242-20
Digits Only 6945224220
Product NDC 69452-242
Product ID 69452-242_38f3f3f8-6374-9981-e063-6294a90aa5df
Description

100 TABLET in 1 BOTTLE (69452-242-20)

Marketing

Marketing Status
Discontinued 2026-03-31
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": "38f3f3f8-6374-9981-e063-6294a90aa5df", "openfda": {"upc": ["0369452242322", "0369452242209", "0369452241202", "0369452241325"], "unii": ["AO61G82577"], "rxcui": ["905269", "905283"], "spl_set_id": ["4d4d473e-4f84-43e7-bb17-49e8dc1e97fd"], "manufacturer_name": ["Bionpharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69452-242-20)", "package_ndc": "69452-242-20", "marketing_end_date": "20260331", "marketing_start_date": "20181215"}], "brand_name": "Trihexyphenidyl Hydrochloride", "product_id": "69452-242_38f3f3f8-6374-9981-e063-6294a90aa5df", "dosage_form": "TABLET", "product_ndc": "69452-242", "generic_name": "Trihexyphenidyl Hydrochloride", "labeler_name": "Bionpharma Inc.", "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_end_date": "20260331", "marketing_start_date": "20181215"}