Package 0641-6238-25

{"route": ["INTRAVENOUS"], "spl_id": "355370f0-4f22-42cf-92c4-fda0763ccc2e", "openfda": {"unii": ["U6X61U5ZEG"], "rxcui": ["1116294"], "spl_set_id": ["794cb942-04e3-4472-8eb8-92613329e4d5"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (0641-6238-25)  / 1 mL in 1 VIAL, SINGLE-DOSE (0641-6238-01)", "package_ndc": "0641-6238-25", "marketing_start_date": "20201215"}], "brand_name": "Ephedrine Sulfate", "product_id": "0641-6238_355370f0-4f22-42cf-92c4-fda0763ccc2e", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "Adrenergic beta-Agonists [MoA]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Releasing Agent [EPC]", "alpha-Adrenergic Agonist [EPC]", "beta-Adrenergic Agonist [EPC]"], "product_ndc": "0641-6238", "generic_name": "Ephedrine Sulfate", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ephedrine Sulfate", "active_ingredients": [{"name": "EPHEDRINE SULFATE", "strength": "50 mg/mL"}], "application_number": "ANDA214334", "marketing_category": "ANDA", "marketing_start_date": "20201215", "listing_expiration_date": "20261231"}