Package 55111-302-30

{"route": ["ORAL"], "spl_id": "0df6bfb2-4604-2035-9677-06c125e77bb9", "openfda": {"upc": ["0355111302308"], "unii": ["3O2T2PJ89D"], "rxcui": ["1100184"], "spl_set_id": ["7c0d3bcb-157d-0414-64ee-055bc614d190"], "manufacturer_name": ["Dr. Reddys Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (55111-302-30)", "package_ndc": "55111-302-30", "marketing_start_date": "20250820"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (55111-302-90)", "package_ndc": "55111-302-90", "marketing_start_date": "20250820"}], "brand_name": "Donepezil hydrochloride", "product_id": "55111-302_0df6bfb2-4604-2035-9677-06c125e77bb9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "55111-302", "generic_name": "Donepezil hydrochloride", "labeler_name": "Dr. Reddys Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Donepezil hydrochloride", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "23 mg/1"}], "application_number": "ANDA202723", "marketing_category": "ANDA", "marketing_start_date": "20250820", "listing_expiration_date": "20261231"}