Package 60687-303-01

Brand: donepezil

Generic: donepezil hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60687-303-01
Digits Only 6068730301
Product NDC 60687-303
Product ID 60687-303_3f922a89-21fe-d605-e063-6294a90a8b8d
Description

100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-303-01) / 1 TABLET in 1 BLISTER PACK (60687-303-11)

Marketing

Marketing Status
Marketed Since 2017-03-21
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": "3f922a89-21fe-d605-e063-6294a90a8b8d", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["997223", "997229"], "spl_set_id": ["12ae85f0-023c-49ca-8c4a-0a6a7585290e"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-303-01)  / 1 TABLET in 1 BLISTER PACK (60687-303-11)", "package_ndc": "60687-303-01", "marketing_start_date": "20170321"}], "brand_name": "Donepezil", "product_id": "60687-303_3f922a89-21fe-d605-e063-6294a90a8b8d", "dosage_form": "TABLET", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "60687-303", "generic_name": "Donepezil hydrochloride", "labeler_name": "American Health Packaging", "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": "20170321", "listing_expiration_date": "20261231"}