Package 62135-671-90

Brand: albuterol sulfate

Generic: albuterol sulfate
NDC Package

Package Facts

Identity

Package NDC 62135-671-90
Digits Only 6213567190
Product NDC 62135-671
Product ID 62135-671_fe7cbf82-9f32-327e-e053-6294a90aebc8
Description

90 TABLET in 1 BOTTLE (62135-671-90)

Marketing

Marketing Status
Marketed Since 2023-06-14
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": ["ORAL"], "spl_id": "fe7cbf82-9f32-327e-e053-6294a90aebc8", "openfda": {"upc": ["0362135672904", "0362135671907"], "unii": ["021SEF3731"], "rxcui": ["197316", "197318"], "spl_set_id": ["81cdae6f-99d7-468b-9ab8-fecb1d42298d"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (62135-671-90)", "package_ndc": "62135-671-90", "marketing_start_date": "20230614"}], "brand_name": "Albuterol Sulfate", "product_id": "62135-671_fe7cbf82-9f32-327e-e053-6294a90aebc8", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "62135-671", "generic_name": "Albuterol Sulfate", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Albuterol Sulfate", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "2 mg/1"}], "application_number": "ANDA072151", "marketing_category": "ANDA", "marketing_start_date": "19891205", "listing_expiration_date": "20261231"}