Package 68788-7996-2
Brand: albuterol sulfate
Generic: albuterol sulfatePackage Facts
Identity
Package NDC
68788-7996-2
Digits Only
6878879962
Product NDC
68788-7996
Description
1 CANISTER in 1 CARTON (68788-7996-2) / 200 AEROSOL, METERED in 1 CANISTER
Marketing
Marketing Status
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": "b4d7b542-5aaa-4a4e-a73a-a2b193715cc8", "openfda": {"unii": ["021SEF3731"], "rxcui": ["2123111"], "spl_set_id": ["d6acb5a7-555a-463a-ae65-2911d6789b42"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 CANISTER in 1 CARTON (68788-7996-2) / 200 AEROSOL, METERED in 1 CANISTER", "package_ndc": "68788-7996-2", "marketing_start_date": "20210810"}], "brand_name": "Albuterol Sulfate", "product_id": "68788-7996_b4d7b542-5aaa-4a4e-a73a-a2b193715cc8", "dosage_form": "AEROSOL, METERED", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "68788-7996", "generic_name": "Albuterol Sulfate", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Albuterol Sulfate", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "108 ug/1"}], "application_number": "NDA020503", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20210810", "listing_expiration_date": "20271231"}