Package 70518-4496-0

Brand: albuterol sulfate

Generic: albuterol sulfate
NDC Package

Package Facts

Identity

Package NDC 70518-4496-0
Digits Only 7051844960
Product NDC 70518-4496
Product ID 70518-4496_40d02383-b4de-f95e-e063-6294a90afdea
Description

1 INHALER in 1 CARTON (70518-4496-0) / 200 INHALANT in 1 INHALER

Marketing

Marketing Status
Marketed Since 2025-10-10
Brand albuterol sulfate
Generic albuterol sulfate
Sample Package No

Linked Drug Pages (1)

Albuterol Sulfate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "40d02383-b4de-f95e-e063-6294a90afdea", "openfda": {"unii": ["021SEF3731"], "rxcui": ["2123072"], "spl_set_id": ["b7c6ae06-b1a8-4bf1-934d-439572e19931"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "1 INHALER in 1 CARTON (70518-4496-0)  / 200 INHALANT in 1 INHALER", "package_ndc": "70518-4496-0", "marketing_start_date": "20251010"}], "brand_name": "Albuterol Sulfate", "product_id": "70518-4496_40d02383-b4de-f95e-e063-6294a90afdea", "dosage_form": "INHALANT", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "70518-4496", "generic_name": "Albuterol Sulfate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Albuterol Sulfate", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "90 ug/1"}], "application_number": "ANDA212447", "marketing_category": "ANDA", "marketing_start_date": "20251010", "listing_expiration_date": "20261231"}