Package 29300-249-01

{"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": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-249-01)", "package_ndc": "29300-249-01", "marketing_start_date": "20180228"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-249-10)", "package_ndc": "29300-249-10", "marketing_start_date": "20180228"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-249-13)", "package_ndc": "29300-249-13", "marketing_start_date": "20180228"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-249-19)", "package_ndc": "29300-249-19", "marketing_start_date": "20180228"}], "brand_name": "donepezil hydrochloride", "product_id": "29300-249_88d3f867-45f4-42fb-93f8-235c2f594760", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "29300-249", "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": "10 mg/1"}], "application_number": "ANDA203656", "marketing_category": "ANDA", "marketing_start_date": "20160623", "listing_expiration_date": "20261231"}