Package 68071-3780-2

Brand: albuterol sulfate

Generic: albuterol sulfate
NDC Package

Package Facts

Identity

Package NDC 68071-3780-2
Digits Only 6807137802
Product NDC 68071-3780
Description

1 POUCH in 1 CARTON (68071-3780-2) / 25 AMPULE in 1 POUCH / 3 mL in 1 AMPULE

Marketing

Marketing Status
Marketed Since 2025-01-21
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": "41afaa31-2e58-8cd4-e063-6294a90af56c", "openfda": {"upc": ["0368071378023"], "unii": ["021SEF3731"], "rxcui": ["630208"], "spl_set_id": ["2c3f975c-dbd8-0362-e063-6394a90a16dd"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 POUCH in 1 CARTON (68071-3780-2)  / 25 AMPULE in 1 POUCH / 3 mL in 1 AMPULE", "package_ndc": "68071-3780-2", "marketing_start_date": "20250121"}], "brand_name": "Albuterol Sulfate", "product_id": "68071-3780_41afaa31-2e58-8cd4-e063-6294a90af56c", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "68071-3780", "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": "ANDA077839", "marketing_category": "ANDA", "marketing_start_date": "20111205", "listing_expiration_date": "20261231"}