Package 42023-243-99
Brand: ephedrine sulfate
Generic: ephedrine sulfatePackage Facts
Identity
Package NDC
42023-243-99
Digits Only
4202324399
Product NDC
42023-243
Description
10 mL in 1 VIAL, SINGLE-DOSE (42023-243-99)
Marketing
Marketing Status
Brand
ephedrine sulfate
Generic
ephedrine sulfate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "b8d2389a-6624-4a8e-bd12-4f62334d7335", "openfda": {"unii": ["U6X61U5ZEG"], "rxcui": ["2368456"], "spl_set_id": ["a247857e-ba7b-4a37-b132-4ba9b0d1c4d1"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 VIAL, SINGLE-DOSE (42023-243-99)", "package_ndc": "42023-243-99", "marketing_start_date": "20240131"}], "brand_name": "EPHEDRINE SULFATE", "product_id": "42023-243_b8d2389a-6624-4a8e-bd12-4f62334d7335", "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": "42023-243", "generic_name": "Ephedrine Sulfate", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "EPHEDRINE SULFATE", "active_ingredients": [{"name": "EPHEDRINE SULFATE", "strength": "5 mg/mL"}], "application_number": "NDA213994", "marketing_category": "NDA", "marketing_start_date": "20240131", "listing_expiration_date": "20261231"}