Package 0591-3870-44

{"route": ["ORAL"], "spl_id": "985e1190-b8a0-4775-9a20-ad1924b14fb2", "openfda": {"unii": ["JY0WD0UA60"], "rxcui": ["996561", "996571", "996572"], "spl_set_id": ["72973b46-f307-4a9e-8fb1-ad2cbccfd736"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BOX, UNIT-DOSE (0591-3870-44)  / 10 TABLET in 1 BLISTER PACK (0591-3870-45)", "package_ndc": "0591-3870-44", "marketing_end_date": "20270930", "marketing_start_date": "20150401"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (0591-3870-60)", "package_ndc": "0591-3870-60", "marketing_end_date": "20280731", "marketing_start_date": "20150401"}], "brand_name": "memantine hydrochloride", "product_id": "0591-3870_985e1190-b8a0-4775-9a20-ad1924b14fb2", "dosage_form": "TABLET", "pharm_class": ["N-methyl-D-aspartate Receptor Antagonist [EPC]", "NMDA Receptor Antagonists [MoA]"], "product_ndc": "0591-3870", "generic_name": "memantine hydrochloride", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "memantine hydrochloride", "active_ingredients": [{"name": "MEMANTINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "NDA021487", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_end_date": "20280731", "marketing_start_date": "20150401"}