Package 70954-211-10

Brand: trihexyphenidyl hydrochloride

Generic: trihexyphenidyl hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70954-211-10
Digits Only 7095421110
Product NDC 70954-211
Product ID 70954-211_83608c13-509d-448b-8559-5f5e8a9a0d75
Description

100 TABLET in 1 BOTTLE (70954-211-10)

Marketing

Marketing Status
Marketed Since 2019-01-28
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": "83608c13-509d-448b-8559-5f5e8a9a0d75", "openfda": {"upc": ["0370954212102", "0370954211105"], "unii": ["AO61G82577"], "rxcui": ["905269", "905283"], "spl_set_id": ["83608c13-509d-448b-8559-5f5e8a9a0d75"], "manufacturer_name": ["Novitium Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70954-211-10)", "package_ndc": "70954-211-10", "marketing_start_date": "20190128"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (70954-211-20)", "package_ndc": "70954-211-20", "marketing_start_date": "20190128"}], "brand_name": "TRIHEXYPHENIDYL HYDROCHLORIDE", "product_id": "70954-211_83608c13-509d-448b-8559-5f5e8a9a0d75", "dosage_form": "TABLET", "product_ndc": "70954-211", "generic_name": "TRIHEXYPHENIDYL HYDROCHLORIDE", "labeler_name": "Novitium Pharma LLC", "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": "20190128", "listing_expiration_date": "20261231"}