Package 70518-3541-0

Brand: albuterol sulfate

Generic: albuterol sulfate
NDC Package

Package Facts

Identity

Package NDC 70518-3541-0
Digits Only 7051835410
Product NDC 70518-3541
Product ID 70518-3541_4456f00c-cd52-1daf-e063-6394a90abb35
Description

1 CANISTER in 1 CARTON (70518-3541-0) / 200 AEROSOL, METERED in 1 CANISTER

Marketing

Marketing Status
Marketed Since 2022-09-28
Brand albuterol sulfate
Generic albuterol sulfate
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "4456f00c-cd52-1daf-e063-6394a90abb35", "openfda": {"unii": ["021SEF3731"], "rxcui": ["2123072"], "spl_set_id": ["0cfb6c5d-eac2-4a1c-8a0f-6b00e819adda"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "1 CANISTER in 1 CARTON (70518-3541-0)  / 200 AEROSOL, METERED in 1 CANISTER", "package_ndc": "70518-3541-0", "marketing_start_date": "20220928"}], "brand_name": "Albuterol sulfate", "product_id": "70518-3541_4456f00c-cd52-1daf-e063-6394a90abb35", "dosage_form": "AEROSOL, METERED", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "70518-3541", "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": "ANDA209954", "marketing_category": "ANDA", "marketing_start_date": "20220928", "listing_expiration_date": "20261231"}