Package 47335-322-88

{"route": ["ORAL"], "spl_id": "81ca8cbf-7854-43a2-bd0b-1dbaf4709a42", "openfda": {"unii": ["JY0WD0UA60"], "rxcui": ["996561", "996571"], "spl_set_id": ["d1963395-3cf7-4433-bf2c-06295bb1c5b0"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (47335-322-08)", "package_ndc": "47335-322-08", "marketing_start_date": "20150711"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (47335-322-13)", "package_ndc": "47335-322-13", "marketing_start_date": "20150711"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (47335-322-18)", "package_ndc": "47335-322-18", "marketing_start_date": "20150711"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (47335-322-83)", "package_ndc": "47335-322-83", "marketing_start_date": "20150711"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (47335-322-86)", "package_ndc": "47335-322-86", "marketing_start_date": "20150711"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (47335-322-88)", "package_ndc": "47335-322-88", "marketing_start_date": "20150711"}], "brand_name": "Memantine Hydrochloride", "product_id": "47335-322_81ca8cbf-7854-43a2-bd0b-1dbaf4709a42", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["N-methyl-D-aspartate Receptor Antagonist [EPC]", "NMDA Receptor Antagonists [MoA]"], "product_ndc": "47335-322", "generic_name": "Memantine Hydrochloride", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Memantine Hydrochloride", "active_ingredients": [{"name": "MEMANTINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA090058", "marketing_category": "ANDA", "marketing_start_date": "20150711", "listing_expiration_date": "20261231"}