Package 50090-2627-0

Brand: donepezil

Generic: donepezil hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-2627-0
Digits Only 5009026270
Product NDC 50090-2627
Product ID 50090-2627_1eda014d-ec3c-4940-a6a2-3dfe24b07712
Description

90 TABLET in 1 BOTTLE (50090-2627-0)

Marketing

Marketing Status
Marketed Since 2016-11-17
Brand donepezil
Generic donepezil hydrochloride
Sample Package No

Linked Drug Pages (1)

Donepezil ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1eda014d-ec3c-4940-a6a2-3dfe24b07712", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["997223", "997229"], "spl_set_id": ["84d8ca68-26f3-4dd5-9dd4-6a7525a30db1"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-2627-0)", "package_ndc": "50090-2627-0", "marketing_start_date": "20161117"}], "brand_name": "Donepezil", "product_id": "50090-2627_1eda014d-ec3c-4940-a6a2-3dfe24b07712", "dosage_form": "TABLET", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "50090-2627", "generic_name": "Donepezil hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Donepezil", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA203034", "marketing_category": "ANDA", "marketing_start_date": "20150202", "listing_expiration_date": "20271231"}