Package 76282-679-42

Brand: albuterol sulfate

Generic: albuterol sulfate
NDC Package

Package Facts

Identity

Package NDC 76282-679-42
Digits Only 7628267942
Product NDC 76282-679
Description

1 CANISTER in 1 CARTON (76282-679-42) / 200 INHALANT in 1 CANISTER

Marketing

Marketing Status
Marketed Since 2021-10-04
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": "3449ab68-28d3-42f5-8d34-329bf6fa0e6b", "openfda": {"upc": ["0376282679426"], "unii": ["021SEF3731"], "rxcui": ["2123111"], "spl_set_id": ["29e35e54-dbd6-4426-993f-893d7a4d69be"], "manufacturer_name": ["Exelan Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 CANISTER in 1 CARTON (76282-679-42)  / 200 INHALANT in 1 CANISTER", "package_ndc": "76282-679-42", "marketing_start_date": "20211004"}], "brand_name": "ALBUTEROL SULFATE", "product_id": "76282-679_3449ab68-28d3-42f5-8d34-329bf6fa0e6b", "dosage_form": "INHALANT", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "76282-679", "generic_name": "albuterol sulfate", "labeler_name": "Exelan Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ALBUTEROL SULFATE", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "90 ug/1"}], "application_number": "ANDA209959", "marketing_category": "ANDA", "marketing_start_date": "20211004", "listing_expiration_date": "20261231"}