Package 43386-480-24

{"route": ["ORAL"], "spl_id": "e80ecc89-bd45-4796-850b-c379a79ac7ab", "openfda": {"unii": ["X0A40N8I4S"], "rxcui": ["994521"], "spl_set_id": ["7b76c8a7-dd0c-481c-8299-26dfd38ce066"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (43386-480-24)", "package_ndc": "43386-480-24", "marketing_start_date": "19980619"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (43386-480-26)", "package_ndc": "43386-480-26", "marketing_start_date": "19980619"}, {"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (43386-480-28)", "package_ndc": "43386-480-28", "marketing_start_date": "19980619"}], "brand_name": "ORPHENADRINE CITRATE", "product_id": "43386-480_e80ecc89-bd45-4796-850b-c379a79ac7ab", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "43386-480", "generic_name": "ORPHENADRINE CITRATE", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ORPHENADRINE CITRATE", "active_ingredients": [{"name": "ORPHENADRINE CITRATE", "strength": "100 mg/1"}], "application_number": "ANDA040284", "marketing_category": "ANDA", "marketing_start_date": "19980619", "listing_expiration_date": "20261231"}