Package 50228-140-30

Brand: donepezil hydrochloride

Generic: donepezil hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50228-140-30
Digits Only 5022814030
Product NDC 50228-140
Description

30 TABLET, FILM COATED in 1 BOTTLE (50228-140-30)

Marketing

Marketing Status
Marketed Since 2014-10-29
Brand donepezil hydrochloride
Generic donepezil hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "652d4a32-9c92-43df-be8a-a91cfaf61c3a", "openfda": {"upc": ["0350228140300", "0350228139106", "0350228139304"], "unii": ["3O2T2PJ89D"], "rxcui": ["997223", "997229"], "spl_set_id": ["6e9aacf9-abb6-4dec-9a8d-4eabf934d512"], "manufacturer_name": ["ScieGen Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (50228-140-10)", "package_ndc": "50228-140-10", "marketing_start_date": "20141029"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50228-140-30)", "package_ndc": "50228-140-30", "marketing_start_date": "20141029"}], "brand_name": "Donepezil Hydrochloride", "product_id": "50228-140_652d4a32-9c92-43df-be8a-a91cfaf61c3a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "50228-140", "generic_name": "Donepezil Hydrochloride", "labeler_name": "ScieGen Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Donepezil Hydrochloride", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA203907", "marketing_category": "ANDA", "marketing_start_date": "20141029", "listing_expiration_date": "20271231"}