Package 51662-1372-1

{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "ef7bd6e6-d631-7e93-e053-2a95a90aef83", "openfda": {"unii": ["SK47B8698T"], "rxcui": ["1658236"], "spl_set_id": ["94e9a33f-39c4-4bc5-e053-2a95a90a43ac"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "20 mL in 1 VIAL, SINGLE-DOSE (51662-1372-1)", "package_ndc": "51662-1372-1", "marketing_start_date": "20191014"}], "brand_name": "MAGNESIUM SULFATE", "product_id": "51662-1372_ef7bd6e6-d631-7e93-e053-2a95a90aef83", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Calculi Dissolution Agent [EPC]", "Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]", "Magnesium Ion Exchange Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "51662-1372", "generic_name": "MAGNESIUM SULFATE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MAGNESIUM SULFATE", "active_ingredients": [{"name": "MAGNESIUM SULFATE HEPTAHYDRATE", "strength": "500 mg/mL"}], "application_number": "NDA019316", "marketing_category": "NDA", "marketing_start_date": "20191014", "listing_expiration_date": "20261231"}