Package 51662-1499-1

Brand: albuterol sulfate

Generic: albuterol sulfate
NDC Package

Package Facts

Identity

Package NDC 51662-1499-1
Digits Only 5166214991
Product NDC 51662-1499
Product ID 51662-1499_2b387337-c48e-7eb1-e063-6294a90a9cba
Description

5 VIAL, SINGLE-DOSE in 1 POUCH (51662-1499-1) / 3 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2020-01-29
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": "2b387337-c48e-7eb1-e063-6294a90a9cba", "openfda": {"upc": ["0304879501003"], "unii": ["021SEF3731"], "rxcui": ["630208"], "spl_set_id": ["9d4ef83f-8ca0-811e-e053-2995a90a6d0d"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "5 VIAL, SINGLE-DOSE in 1 POUCH (51662-1499-1)  / 3 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "51662-1499-1", "marketing_start_date": "20200129"}], "brand_name": "ALBUTEROL SULFATE", "product_id": "51662-1499_2b387337-c48e-7eb1-e063-6294a90a9cba", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "51662-1499", "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": "2.5 mg/3mL"}], "application_number": "ANDA074880", "marketing_category": "ANDA", "marketing_start_date": "20200129", "listing_expiration_date": "20261231"}