Package 0591-5335-10

Brand: trihexyphenidyl hydrochloride

Generic: trihexyphenidyl hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0591-5335-10
Digits Only 0591533510
Product NDC 0591-5335
Description

1000 TABLET in 1 BOTTLE, PLASTIC (0591-5335-10)

Marketing

Marketing Status
Marketed Since 1987-11-01
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": "0b42f7c5-1597-46fd-bc35-5f9286d27877", "openfda": {"unii": ["AO61G82577"], "rxcui": ["905269", "905283"], "spl_set_id": ["a44d7803-164d-4a67-9356-581c45de8596"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (0591-5335-01)", "package_ndc": "0591-5335-01", "marketing_start_date": "19871101"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (0591-5335-10)", "package_ndc": "0591-5335-10", "marketing_start_date": "19871101"}], "brand_name": "Trihexyphenidyl Hydrochloride", "product_id": "0591-5335_0b42f7c5-1597-46fd-bc35-5f9286d27877", "dosage_form": "TABLET", "product_ndc": "0591-5335", "generic_name": "Trihexyphenidyl Hydrochloride", "labeler_name": "Actavis Pharma, 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": "19871101", "listing_expiration_date": "20261231"}