Package 63187-401-30

Brand: donepezil hydrochloride

Generic: donepezil hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63187-401-30
Digits Only 6318740130
Product NDC 63187-401
Product ID 63187-401_531ec397-a99e-44f3-8c1f-52929a70359a
Description

30 TABLET, FILM COATED in 1 BOTTLE (63187-401-30)

Marketing

Marketing Status
Marketed Since 2019-01-01
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": "531ec397-a99e-44f3-8c1f-52929a70359a", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["997223"], "spl_set_id": ["31d6a5a0-eaf0-4c7c-8d50-742ae520cca9"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63187-401-30)", "package_ndc": "63187-401-30", "marketing_start_date": "20190101"}], "brand_name": "DONEPEZIL HYDROCHLORIDE", "product_id": "63187-401_531ec397-a99e-44f3-8c1f-52929a70359a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "63187-401", "generic_name": "DONEPEZIL HYDROCHLORIDE", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DONEPEZIL HYDROCHLORIDE", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA090768", "marketing_category": "ANDA", "marketing_start_date": "20110529", "listing_expiration_date": "20261231"}