Package 0074-4456-51
Brand: ultane
Generic: sevofluranePackage Facts
Identity
Package NDC
0074-4456-51
Digits Only
0074445651
Product NDC
0074-4456
Description
250 mL in 1 BOTTLE, PLASTIC (0074-4456-51)
Marketing
Marketing Status
Brand
ultane
Generic
sevoflurane
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "4b7ba14d-8de1-4f87-910e-87fdd984b24d", "openfda": {"nui": ["N0000175975", "N0000175681"], "unii": ["38LVP0K73A"], "rxcui": ["200243", "541963"], "spl_set_id": ["c9aa6489-5a36-44ed-9512-b996833d82f7"], "pharm_class_pe": ["General Anesthesia [PE]"], "pharm_class_epc": ["General Anesthetic [EPC]"], "manufacturer_name": ["AbbVie Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "250 mL in 1 BOTTLE, PLASTIC (0074-4456-51)", "package_ndc": "0074-4456-51", "marketing_start_date": "19950607"}], "brand_name": "Ultane", "product_id": "0074-4456_4b7ba14d-8de1-4f87-910e-87fdd984b24d", "dosage_form": "LIQUID", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "0074-4456", "generic_name": "Sevoflurane", "labeler_name": "AbbVie Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ultane", "active_ingredients": [{"name": "SEVOFLURANE", "strength": "250 mL/250mL"}], "application_number": "NDA020478", "marketing_category": "NDA", "marketing_start_date": "19950607", "listing_expiration_date": "20261231"}