Package 70518-2072-0

Brand: albuterol sulate hfa

Generic: albuterol sulfate
NDC Package

Package Facts

Identity

Package NDC 70518-2072-0
Digits Only 7051820720
Product NDC 70518-2072
Product ID 70518-2072_499c75ab-2f45-5ba7-e063-6394a90aecfc
Description

1 INHALER in 1 CARTON (70518-2072-0) / 200 AEROSOL, METERED in 1 INHALER

Marketing

Marketing Status
Marketed Since 2019-05-13
Brand albuterol sulate hfa
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": "499c75ab-2f45-5ba7-e063-6394a90aecfc", "openfda": {"unii": ["021SEF3731"], "rxcui": ["2123076"], "spl_set_id": ["77d34a3c-ccc6-420a-ad31-a1af55f7de76"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "1 INHALER in 1 CARTON (70518-2072-0)  / 200 AEROSOL, METERED in 1 INHALER", "package_ndc": "70518-2072-0", "marketing_start_date": "20190513"}], "brand_name": "Albuterol Sulate HFA", "product_id": "70518-2072_499c75ab-2f45-5ba7-e063-6394a90aecfc", "dosage_form": "AEROSOL, METERED", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "70518-2072", "generic_name": "albuterol sulfate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Albuterol Sulate", "brand_name_suffix": "HFA", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "90 ug/1"}], "application_number": "NDA020983", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20190513", "listing_expiration_date": "20271231"}