Package 0904-6505-61

{"route": ["ORAL"], "spl_id": "f98561aa-0a02-4e99-bacb-d92c81833bbe", "openfda": {"unii": ["JY0WD0UA60"], "rxcui": ["996561", "996571"], "spl_set_id": ["d0a5e0fc-04e3-417d-bef3-9b309ff71597"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 CARTON (0904-6505-06)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-6505-06", "marketing_start_date": "20150720"}, {"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6505-61)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-6505-61", "marketing_start_date": "20150720"}], "brand_name": "Memantine Hydrochloride", "product_id": "0904-6505_f98561aa-0a02-4e99-bacb-d92c81833bbe", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["N-methyl-D-aspartate Receptor Antagonist [EPC]", "NMDA Receptor Antagonists [MoA]"], "product_ndc": "0904-6505", "generic_name": "Memantine Hydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Memantine Hydrochloride", "active_ingredients": [{"name": "MEMANTINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA090048", "marketing_category": "ANDA", "marketing_start_date": "20150720", "listing_expiration_date": "20261231"}