Package 70518-1081-0

Brand: ventolin hfa

Generic: albuterol sulfate
NDC Package

Package Facts

Identity

Package NDC 70518-1081-0
Digits Only 7051810810
Product NDC 70518-1081
Product ID 70518-1081_485918a3-f680-2d1c-e063-6294a90a00e9
Description

200 AEROSOL, METERED in 1 INHALER (70518-1081-0)

Marketing

Marketing Status
Marketed Since 2018-03-24
Brand ventolin hfa
Generic albuterol sulfate
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "485918a3-f680-2d1c-e063-6294a90a00e9", "openfda": {"unii": ["021SEF3731"], "rxcui": ["859088", "2123076"], "spl_set_id": ["adb8d669-b91c-46f1-8a86-19f504840eff"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "200 AEROSOL, METERED in 1 INHALER (70518-1081-0)", "package_ndc": "70518-1081-0", "marketing_start_date": "20180324"}], "brand_name": "VENTOLIN HFA", "product_id": "70518-1081_485918a3-f680-2d1c-e063-6294a90a00e9", "dosage_form": "AEROSOL, METERED", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "70518-1081", "generic_name": "albuterol sulfate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VENTOLIN", "brand_name_suffix": "HFA", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "90 ug/1"}], "application_number": "NDA020983", "marketing_category": "NDA", "marketing_start_date": "20180324", "listing_expiration_date": "20271231"}