Package 51662-1513-1

Brand: albuterol sulfate

Generic: albuterol sulfate
NDC Package

Package Facts

Identity

Package NDC 51662-1513-1
Digits Only 5166215131
Product NDC 51662-1513
Product ID 51662-1513_ef7c1f9d-3076-5fc6-e053-2a95a90aafec
Description

1 INHALER in 1 CARTON (51662-1513-1) / 200 AEROSOL, METERED in 1 INHALER

Marketing

Marketing Status
Marketed Since 2020-08-18
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": "ef7c1f9d-3076-5fc6-e053-2a95a90aafec", "openfda": {"unii": ["021SEF3731"], "rxcui": ["2123072"], "spl_set_id": ["ad299502-8779-d280-e053-2995a90a7371"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "1 INHALER in 1 CARTON (51662-1513-1)  / 200 AEROSOL, METERED in 1 INHALER", "package_ndc": "51662-1513-1", "marketing_start_date": "20200818"}], "brand_name": "ALBUTEROL SULFATE", "product_id": "51662-1513_ef7c1f9d-3076-5fc6-e053-2a95a90aafec", "dosage_form": "AEROSOL, METERED", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "51662-1513", "generic_name": "ALBUTEROL SULFATE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ALBUTEROL SULFATE", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "90 ug/1"}], "application_number": "ANDA203760", "marketing_category": "ANDA", "marketing_start_date": "20200818", "listing_expiration_date": "20261231"}