Package 71335-2907-1

Brand: albuterol sulfate

Generic: albuterol sulfate
NDC Package

Package Facts

Identity

Package NDC 71335-2907-1
Digits Only 7133529071
Product NDC 71335-2907
Product ID 71335-2907_474dd04b-2935-4af1-a309-958c00f08193
Description

473 mL in 1 BOTTLE (71335-2907-1)

Marketing

Marketing Status
Marketed Since 2025-11-10
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": ["ORAL"], "spl_id": "474dd04b-2935-4af1-a309-958c00f08193", "openfda": {"unii": ["021SEF3731"], "rxcui": ["755497"], "spl_set_id": ["378461f2-7271-44a3-9da3-b39970b65d3a"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (71335-2907-1)", "package_ndc": "71335-2907-1", "marketing_start_date": "20251110"}], "brand_name": "ALBUTEROL SULFATE", "product_id": "71335-2907_474dd04b-2935-4af1-a309-958c00f08193", "dosage_form": "SYRUP", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "71335-2907", "generic_name": "ALBUTEROL SULFATE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ALBUTEROL SULFATE", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "2 mg/5mL"}], "application_number": "ANDA212197", "marketing_category": "ANDA", "marketing_start_date": "20190906", "listing_expiration_date": "20261231"}