Package 68071-4754-2

Brand: albuterol sulfate

Generic: albuterol sulfate
NDC Package

Package Facts

Identity

Package NDC 68071-4754-2
Digits Only 6807147542
Product NDC 68071-4754
Product ID 68071-4754_2d7cdf76-7c87-8de1-e063-6394a90a0c2c
Description

3 mL in 1 VIAL, SINGLE-DOSE (68071-4754-2)

Marketing

Marketing Status
Marketed Since 2019-02-06
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": "2d7cdf76-7c87-8de1-e063-6394a90a0c2c", "openfda": {"upc": ["0368071475425"], "unii": ["021SEF3731"], "rxcui": ["630208"], "spl_set_id": ["813d49be-3651-6759-e053-2991aa0a6a9f"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "3 mL in 1 VIAL, SINGLE-DOSE (68071-4754-2)", "package_ndc": "68071-4754-2", "marketing_start_date": "20190206"}], "brand_name": "Albuterol Sulfate", "product_id": "68071-4754_2d7cdf76-7c87-8de1-e063-6394a90a0c2c", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "68071-4754", "generic_name": "Albuterol Sulfate", "labeler_name": "NuCare Pharmaceuticals,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"}