Package 68180-159-01

{"route": ["ORAL"], "spl_id": "c8158f85-c286-402d-9cca-85bcfe4e4085", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["M5DP350VZV"], "rxcui": ["1251903"], "spl_set_id": ["358dd0c5-4d89-403e-9428-a785ec862869"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68180-159-01)", "package_ndc": "68180-159-01", "marketing_start_date": "20200224"}], "brand_name": "Ethacrynic Acid", "product_id": "68180-159_c8158f85-c286-402d-9cca-85bcfe4e4085", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "68180-159", "generic_name": "Ethacrynic Acid", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ethacrynic Acid", "active_ingredients": [{"name": "ETHACRYNIC ACID", "strength": "25 mg/1"}], "application_number": "ANDA211719", "marketing_category": "ANDA", "marketing_start_date": "20200224", "listing_expiration_date": "20261231"}