Package 43063-659-30

Brand: donepezil hydrochloride

Generic: donepezil hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43063-659-30
Digits Only 4306365930
Product NDC 43063-659
Product ID 43063-659_4139fb45-0028-88cf-e063-6294a90af3db
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-659-30)

Marketing

Marketing Status
Marketed Since 2016-03-04
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": "4139fb45-0028-88cf-e063-6294a90af3db", "openfda": {"upc": ["0343063659908"], "unii": ["3O2T2PJ89D"], "rxcui": ["997223"], "spl_set_id": ["2be9f49d-e7db-4846-e054-00144ff8d46c"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-659-30)", "package_ndc": "43063-659-30", "marketing_start_date": "20160304"}], "brand_name": "Donepezil Hydrochloride", "product_id": "43063-659_4139fb45-0028-88cf-e063-6294a90af3db", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "43063-659", "generic_name": "Donepezil Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Donepezil Hydrochloride", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA201146", "marketing_category": "ANDA", "marketing_start_date": "20120817", "listing_expiration_date": "20261231"}