Package 0121-0658-16

Brand: trihexyphenidyl hydrochloride

Generic: trihexyphenidyl hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0121-0658-16
Digits Only 0121065816
Product NDC 0121-0658
Product ID 0121-0658_e3815d2f-f3ee-4cd6-8a2d-518c74787152
Description

473 mL in 1 BOTTLE (0121-0658-16)

Marketing

Marketing Status
Marketed Since 1997-05-15
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": "e3815d2f-f3ee-4cd6-8a2d-518c74787152", "openfda": {"unii": ["AO61G82577"], "rxcui": ["905273"], "spl_set_id": ["9036c9f0-6d2d-4d0f-a20e-e36f9be228f7"], "manufacturer_name": ["PAI Holdings, LLC dba PAI Pharma"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (0121-0658-16)", "package_ndc": "0121-0658-16", "marketing_start_date": "19970515"}], "brand_name": "Trihexyphenidyl Hydrochloride", "product_id": "0121-0658_e3815d2f-f3ee-4cd6-8a2d-518c74787152", "dosage_form": "SOLUTION", "product_ndc": "0121-0658", "generic_name": "Trihexyphenidyl Hydrochloride", "labeler_name": "PAI Holdings, LLC dba PAI Pharma", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trihexyphenidyl Hydrochloride", "active_ingredients": [{"name": "TRIHEXYPHENIDYL HYDROCHLORIDE", "strength": "2 mg/5mL"}], "application_number": "ANDA040177", "marketing_category": "ANDA", "marketing_start_date": "19970515", "listing_expiration_date": "20261231"}