Package 72189-031-30

Brand: donepezil hydrochloride

Generic: donepezil hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72189-031-30
Digits Only 7218903130
Product NDC 72189-031
Product ID 72189-031_2c4e974d-41bb-49ca-e063-6394a90ae3a0
Description

30 TABLET, FILM COATED in 1 BOTTLE (72189-031-30)

Marketing

Marketing Status
Marketed Since 2019-10-01
Brand donepezil hydrochloride
Generic donepezil hydrochloride
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c4e974d-41bb-49ca-e063-6394a90ae3a0", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["997229"], "spl_set_id": ["93dddf28-094b-dd8c-e053-2995a90a63e9"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-031-30)", "package_ndc": "72189-031-30", "marketing_start_date": "20191001"}], "brand_name": "DONEPEZIL HYDROCHLORIDE", "product_id": "72189-031_2c4e974d-41bb-49ca-e063-6394a90ae3a0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "72189-031", "generic_name": "DONEPEZIL HYDROCHLORIDE", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DONEPEZIL HYDROCHLORIDE", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA200292", "marketing_category": "ANDA", "marketing_start_date": "20191001", "listing_expiration_date": "20261231"}