Package 68788-8787-2

Brand: albuterol sulfate

Generic: albuterol sulfate
NDC Package

Package Facts

Identity

Package NDC 68788-8787-2
Digits Only 6878887872
Product NDC 68788-8787
Description

1 CANISTER in 1 CARTON (68788-8787-2) / 200 AEROSOL, METERED in 1 CANISTER

Marketing

Marketing Status
Marketed Since 2024-12-16
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": "bf0a6eed-8b08-4cc6-92be-328fd627ea89", "openfda": {"unii": ["021SEF3731"], "rxcui": ["2123111"], "spl_set_id": ["1f0bf143-66d4-4a39-b2d1-a5c460ffdcf9"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 CANISTER in 1 CARTON (68788-8787-2)  / 200 AEROSOL, METERED in 1 CANISTER", "package_ndc": "68788-8787-2", "marketing_start_date": "20241216"}], "brand_name": "Albuterol Sulfate", "product_id": "68788-8787_bf0a6eed-8b08-4cc6-92be-328fd627ea89", "dosage_form": "AEROSOL, METERED", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "68788-8787", "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": "90 ug/1"}], "application_number": "ANDA207085", "marketing_category": "ANDA", "marketing_start_date": "20241216", "listing_expiration_date": "20271231"}