Package 68071-4543-6

Brand: albuterol sulfate

Generic: albuterol sulfate
NDC Package

Package Facts

Identity

Package NDC 68071-4543-6
Digits Only 6807145436
Product NDC 68071-4543
Description

3 mL in 1 CONTAINER (68071-4543-6)

Marketing

Marketing Status
Marketed Since 2018-08-29
Brand albuterol sulfate
Generic albuterol sulfate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "2b3707fa-ceec-d6c9-e063-6294a90a1cc0", "openfda": {"upc": ["0368071454369"], "unii": ["021SEF3731"], "rxcui": ["630208"], "spl_set_id": ["749992b4-69e0-0cc8-e053-2991aa0aeb25"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "3 mL in 1 CONTAINER (68071-4543-6)", "package_ndc": "68071-4543-6", "marketing_start_date": "20180829"}], "brand_name": "Albuterol Sulfate", "product_id": "68071-4543_2b3707fa-ceec-d6c9-e063-6294a90a1cc0", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "68071-4543", "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"}