Package 25021-836-01
Brand: ephedrine sulfate
Generic: ephedrine sulfatePackage Facts
Identity
Package NDC
25021-836-01
Digits Only
2502183601
Product NDC
25021-836
Description
25 VIAL in 1 CARTON (25021-836-01) / 1 mL in 1 VIAL
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": "0cced8a7-58b3-43e5-afca-2d6d3ed4c017", "openfda": {"unii": ["U6X61U5ZEG"], "rxcui": ["1116294"], "spl_set_id": ["614e6649-a0e1-4428-855b-363abdb126d8"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (25021-836-01) / 1 mL in 1 VIAL", "package_ndc": "25021-836-01", "marketing_start_date": "20230415"}], "brand_name": "Ephedrine Sulfate", "product_id": "25021-836_0cced8a7-58b3-43e5-afca-2d6d3ed4c017", "dosage_form": "INJECTION, SOLUTION", "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": "25021-836", "generic_name": "Ephedrine Sulfate", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ephedrine Sulfate", "active_ingredients": [{"name": "EPHEDRINE SULFATE", "strength": "50 mg/mL"}], "application_number": "ANDA214528", "marketing_category": "ANDA", "marketing_start_date": "20230415", "listing_expiration_date": "20261231"}