Package 68180-527-06
Brand: donepezil hydrochloride
Generic: donepezil hydrochloridePackage Facts
Identity
Package NDC
68180-527-06
Digits Only
6818052706
Product NDC
68180-527
Description
30 TABLET in 1 BOTTLE (68180-527-06)
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": "f8867ea9-a608-4b0f-9052-fa5c44d7e7c2", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["1100184"], "spl_set_id": ["03e26183-3e07-45e8-a414-a8bad32483e2"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68180-527-06)", "package_ndc": "68180-527-06", "marketing_start_date": "20151221"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68180-527-09)", "package_ndc": "68180-527-09", "marketing_start_date": "20151221"}], "brand_name": "DONEPEZIL HYDROCHLORIDE", "product_id": "68180-527_f8867ea9-a608-4b0f-9052-fa5c44d7e7c2", "dosage_form": "TABLET", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "68180-527", "generic_name": "DONEPEZIL HYDROCHLORIDE", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DONEPEZIL HYDROCHLORIDE", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "23 mg/1"}], "application_number": "ANDA202782", "marketing_category": "ANDA", "marketing_start_date": "20151221", "listing_expiration_date": "20261231"}