Package 70518-1666-0

Brand: donepezil hydrochloride

Generic: donepezil hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-1666-0
Digits Only 7051816660
Product NDC 70518-1666
Product ID 70518-1666_49609e24-52fa-f424-e063-6294a90a1e0e
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1666-0)

Marketing

Marketing Status
Marketed Since 2018-11-12
Brand donepezil hydrochloride
Generic donepezil hydrochloride
Sample Package No

Linked Drug Pages (1)

donepezil hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "49609e24-52fa-f424-e063-6294a90a1e0e", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["997223"], "spl_set_id": ["41c095b6-acd9-4627-a813-bbca7ecafee5"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1666-0)", "package_ndc": "70518-1666-0", "marketing_start_date": "20181112"}], "brand_name": "donepezil hydrochloride", "product_id": "70518-1666_49609e24-52fa-f424-e063-6294a90a1e0e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "70518-1666", "generic_name": "donepezil hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "donepezil hydrochloride", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA200292", "marketing_category": "ANDA", "marketing_start_date": "20181112", "listing_expiration_date": "20271231"}