Package 42799-954-02
Brand: donepezil hydrochloride
Generic: donepezil hydrochloridePackage Facts
Identity
Package NDC
42799-954-02
Digits Only
4279995402
Product NDC
42799-954
Description
90 TABLET, FILM COATED in 1 BOTTLE (42799-954-02)
Marketing
Marketing Status
Brand
donepezil hydrochloride
Generic
donepezil hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "19147d81-49ac-463e-8643-26dace803ea5", "openfda": {"upc": ["0342799954028", "0342799954011"], "unii": ["3O2T2PJ89D"], "rxcui": ["1100184"], "spl_set_id": ["11404dc3-1bde-4d4e-8386-006b67ee19dd"], "manufacturer_name": ["Edenbridge Pharmaceuticals LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (42799-954-01)", "package_ndc": "42799-954-01", "marketing_start_date": "20231205"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (42799-954-02)", "package_ndc": "42799-954-02", "marketing_start_date": "20231205"}], "brand_name": "Donepezil hydrochloride", "product_id": "42799-954_19147d81-49ac-463e-8643-26dace803ea5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "42799-954", "generic_name": "Donepezil hydrochloride", "labeler_name": "Edenbridge Pharmaceuticals LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Donepezil hydrochloride", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "23 mg/1"}], "application_number": "ANDA203713", "marketing_category": "ANDA", "marketing_start_date": "20160219", "listing_expiration_date": "20261231"}