Package 33342-030-60
Brand: donepezil hydrochloride
Generic: donepezil hydrochloridePackage Facts
Identity
Package NDC
33342-030-60
Digits Only
3334203060
Product NDC
33342-030
Description
4 BLISTER PACK in 1 CARTON (33342-030-60) / 7 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Marketing
Marketing Status
Brand
donepezil hydrochloride
Generic
donepezil hydrochloride
Sample Package
No
Linked Drug Pages (0)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4bf742a3-3c8f-4bd3-b973-54370cbef345", "openfda": {"upc": ["0333342061102", "0333342061072", "0333342030078", "0333342027108", "0333342027078", "0333342029072", "0333342029607", "0333342027153", "0333342028150", "0333342030603"], "unii": ["3O2T2PJ89D"], "rxcui": ["997220", "997223", "997226", "997229", "1100184"], "spl_set_id": ["06dd25a5-1bf2-446d-ad75-ff9d55117660"], "manufacturer_name": ["Macleods Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (33342-030-06) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK", "package_ndc": "33342-030-06", "marketing_start_date": "20121214"}, {"sample": false, "description": "30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (33342-030-07)", "package_ndc": "33342-030-07", "marketing_start_date": "20121214"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (33342-030-12) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK", "package_ndc": "33342-030-12", "marketing_start_date": "20121214"}, {"sample": false, "description": "4 BLISTER PACK in 1 CARTON (33342-030-60) / 7 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK", "package_ndc": "33342-030-60", "marketing_start_date": "20121214"}], "brand_name": "Donepezil Hydrochloride", "product_id": "33342-030_4bf742a3-3c8f-4bd3-b973-54370cbef345", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "33342-030", "generic_name": "Donepezil Hydrochloride", "labeler_name": "Macleods Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Donepezil Hydrochloride", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA201787", "marketing_category": "ANDA", "marketing_start_date": "20121214", "listing_expiration_date": "20261231"}