Package 0023-1145-02

{"route": ["INTRADERMAL", "INTRAMUSCULAR"], "spl_id": "7365af65-15e0-4fc1-aa6a-aaec5a43c468", "openfda": {"nui": ["N0000175771", "N0000193962", "N0000175731", "N0000175770"], "unii": ["E211KPY694"], "rxcui": ["860192", "860195", "897366", "897368"], "spl_set_id": ["33d066a9-34ff-4a1a-b38b-d10983df3300"], "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 in 1 CARTON (0023-1145-01)  / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL", "package_ndc": "0023-1145-01", "marketing_start_date": "19891215"}, {"sample": false, "description": "1 VIAL in 1 CARTON (0023-1145-02)  / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL", "package_ndc": "0023-1145-02", "marketing_start_date": "19891215"}], "brand_name": "BOTOX", "product_id": "0023-1145_7365af65-15e0-4fc1-aa6a-aaec5a43c468", "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": "0023-1145", "generic_name": "onabotulinumtoxinA", "labeler_name": "Allergan, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BOTOX", "active_ingredients": [{"name": "BOTULINUM TOXIN TYPE A", "strength": "100 [USP'U]/1"}], "application_number": "BLA103000", "marketing_category": "BLA", "marketing_start_date": "19891215", "listing_expiration_date": "20261231"}