desflurane
Generic: desflurane
Labeler: sandoz inc.Drug Facts
Product Profile
Brand Name
desflurane
Generic Name
desflurane
Labeler
sandoz inc.
Dosage Form
LIQUID
Routes
Active Ingredients
desflurane 240 mL/240mL
Manufacturer
Identifiers & Regulatory
Product NDC
0781-6172
Product ID
0781-6172_ecf9968e-58b0-4792-e053-2995a90aef25
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208234
Listing Expiration
2026-12-31
Marketing Start
2018-02-26
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
07816172
Hyphenated Format
0781-6172
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
desflurane (source: ndc)
Generic Name
desflurane (source: ndc)
Application Number
ANDA208234 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 240 mL/240mL
Packaging
- 6 BOTTLE, GLASS in 1 CARTON (0781-6172-86) / 240 mL in 1 BOTTLE, GLASS (0781-6172-22)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "ecf9968e-58b0-4792-e053-2995a90aef25", "openfda": {"nui": ["N0000175975", "N0000175681"], "upc": ["0307816172229"], "unii": ["CRS35BZ94Q"], "rxcui": ["562366"], "spl_set_id": ["21ba0e18-3dbc-4feb-a3a4-f6470c00910a"], "pharm_class_pe": ["General Anesthesia [PE]"], "pharm_class_epc": ["General Anesthetic [EPC]"], "manufacturer_name": ["Sandoz Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 BOTTLE, GLASS in 1 CARTON (0781-6172-86) / 240 mL in 1 BOTTLE, GLASS (0781-6172-22)", "package_ndc": "0781-6172-86", "marketing_start_date": "20180226"}], "brand_name": "Desflurane", "product_id": "0781-6172_ecf9968e-58b0-4792-e053-2995a90aef25", "dosage_form": "LIQUID", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "0781-6172", "generic_name": "desflurane", "labeler_name": "Sandoz Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desflurane", "active_ingredients": [{"name": "DESFLURANE", "strength": "240 mL/240mL"}], "application_number": "ANDA208234", "marketing_category": "ANDA", "marketing_start_date": "20180226", "listing_expiration_date": "20261231"}