Package 76420-087-03

Brand: albuterol sulfate

Generic: albuterol sulfate
NDC Package

Package Facts

Identity

Package NDC 76420-087-03
Digits Only 7642008703
Product NDC 76420-087
Product ID 76420-087_b1c30e22-3079-11d3-e053-2a95a90a00bf
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (76420-087-03) / 3 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2020-10-16
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": "b1c30e22-3079-11d3-e053-2a95a90a00bf", "openfda": {"unii": ["021SEF3731"], "rxcui": ["630208"], "spl_set_id": ["8153d82c-b5c5-4aa2-bce5-b69cf2d23f5d"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (76420-087-03)  / 3 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "76420-087-03", "marketing_start_date": "20201016"}], "brand_name": "Albuterol Sulfate", "product_id": "76420-087_b1c30e22-3079-11d3-e053-2a95a90a00bf", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "76420-087", "generic_name": "Albuterol Sulfate", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Albuterol Sulfate", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "2.5 mg/3mL"}], "application_number": "ANDA074880", "marketing_category": "ANDA", "marketing_start_date": "19970917", "listing_expiration_date": "20261231"}