Package 0023-9232-01

{"route": ["INTRAMUSCULAR"], "spl_id": "265710db-c7b9-42ff-9fc8-c24a936c1d87", "openfda": {"nui": ["N0000175771", "N0000193962", "N0000175731", "N0000175770"], "upc": ["0300239232013"], "unii": ["E211KPY694"], "rxcui": ["860192", "1726293", "1726296", "1726313"], "spl_set_id": ["485d9b71-6881-42c5-a620-a4360c7192ab"], "pharm_class_pe": ["Neuromuscular Blockade [PE]"], "pharm_class_epc": ["Acetylcholine Release Inhibitor [EPC]", "Neuromuscular Blocker [EPC]"], "pharm_class_moa": ["Acetylcholine Release Inhibitors [MoA]"], "manufacturer_name": ["Allergan, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, GLASS in 1 CARTON (0023-9232-01)  / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, GLASS", "package_ndc": "0023-9232-01", "marketing_start_date": "20080520"}, {"sample": false, "description": "1 VIAL, GLASS in 1 CARTON (0023-9232-02)  / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, GLASS", "package_ndc": "0023-9232-02", "marketing_start_date": "20080520"}], "brand_name": "BOTOX Cosmetic", "product_id": "0023-9232_265710db-c7b9-42ff-9fc8-c24a936c1d87", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Acetylcholine Release Inhibitor [EPC]", "Acetylcholine Release Inhibitors [MoA]", "Neuromuscular Blockade [PE]", "Neuromuscular Blocker [EPC]"], "product_ndc": "0023-9232", "generic_name": "onabotulinumtoxinA", "labeler_name": "Allergan, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BOTOX Cosmetic", "active_ingredients": [{"name": "BOTULINUM TOXIN TYPE A", "strength": "100 [USP'U]/1"}], "application_number": "BLA103000", "marketing_category": "BLA", "marketing_start_date": "20080520", "listing_expiration_date": "20271231"}