Package 50742-392-25

Brand: albuterol sulfate

Generic: albuterol sulfate
NDC Package

Package Facts

Identity

Package NDC 50742-392-25
Digits Only 5074239225
Product NDC 50742-392
Description

5 POUCH in 1 CARTON (50742-392-25) / 5 VIAL in 1 POUCH (50742-392-05) / 3 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2024-11-01
Brand albuterol sulfate
Generic albuterol sulfate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "250b033d-3ed5-c0d1-e063-6394a90a93c9", "openfda": {"upc": ["0350742393053", "0350742392056"], "unii": ["021SEF3731"], "rxcui": ["351136", "351137"], "spl_set_id": ["e14f5fd6-d01a-489d-9baa-61778b1352a8"], "manufacturer_name": ["Ingenus Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 POUCH in 1 CARTON (50742-392-25)  / 5 VIAL in 1 POUCH (50742-392-05)  / 3 mL in 1 VIAL", "package_ndc": "50742-392-25", "marketing_start_date": "20241101"}], "brand_name": "Albuterol Sulfate", "product_id": "50742-392_250b033d-3ed5-c0d1-e063-6394a90a93c9", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "50742-392", "generic_name": "Albuterol Sulfate", "labeler_name": "Ingenus Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Albuterol Sulfate", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": ".63 mg/3mL"}], "application_number": "ANDA215571", "marketing_category": "ANDA", "marketing_start_date": "20241101", "listing_expiration_date": "20261231"}