Package 29300-250-87
Brand: donepezil hydrochloride
Generic: donepezil hydrochloridePackage Facts
Identity
Package NDC
29300-250-87
Digits Only
2930025087
Product NDC
29300-250
Description
3 BLISTER PACK in 1 CARTON (29300-250-87) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (29300-250-11)
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": "88d3f867-45f4-42fb-93f8-235c2f594760", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["997220", "997223", "997226", "997229"], "spl_set_id": ["1a8906ce-96dc-4bc8-81c1-5db67a187aac"], "manufacturer_name": ["Unichem Pharmaceuticals (USA), Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (29300-250-87) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (29300-250-11)", "package_ndc": "29300-250-87", "marketing_start_date": "20180228"}], "brand_name": "donepezil hydrochloride", "product_id": "29300-250_88d3f867-45f4-42fb-93f8-235c2f594760", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "29300-250", "generic_name": "donepezil hydrochloride", "labeler_name": "Unichem Pharmaceuticals (USA), Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "donepezil hydrochloride", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA204831", "marketing_category": "ANDA", "marketing_start_date": "20161110", "listing_expiration_date": "20261231"}