Package 70518-1140-0

Brand: trihexyphenidyl hydrochloride

Generic: trihexyphenidyl hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-1140-0
Digits Only 7051811400
Product NDC 70518-1140
Product ID 70518-1140_485b95c5-2a90-3aa3-e063-6394a90a10d7
Description

30 TABLET in 1 BLISTER PACK (70518-1140-0)

Marketing

Marketing Status
Marketed Since 2018-04-26
Brand trihexyphenidyl hydrochloride
Generic trihexyphenidyl hydrochloride
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "485b95c5-2a90-3aa3-e063-6394a90a10d7", "openfda": {"unii": ["AO61G82577"], "rxcui": ["905283"], "spl_set_id": ["3ed3cdf1-1745-4c6f-bb90-fb7d9471270d"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-1140-0)", "package_ndc": "70518-1140-0", "marketing_start_date": "20180426"}], "brand_name": "Trihexyphenidyl Hydrochloride", "product_id": "70518-1140_485b95c5-2a90-3aa3-e063-6394a90a10d7", "dosage_form": "TABLET", "product_ndc": "70518-1140", "generic_name": "Trihexyphenidyl Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trihexyphenidyl Hydrochloride", "active_ingredients": [{"name": "TRIHEXYPHENIDYL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA084364", "marketing_category": "ANDA", "marketing_start_date": "20180426", "listing_expiration_date": "20271231"}