sevoflurane
Generic: sevoflurane
Labeler: baxter healthcare companyDrug Facts
Product Profile
Brand Name
sevoflurane
Generic Name
sevoflurane
Labeler
baxter healthcare company
Dosage Form
LIQUID
Routes
Active Ingredients
sevoflurane 250 mL/250mL
Manufacturer
Identifiers & Regulatory
Product NDC
10019-651
Product ID
10019-651_51e533f0-ea5a-4210-8fa9-11c1897093a6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA075895
Listing Expiration
2027-12-31
Marketing Start
2002-07-02
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
10019651
Hyphenated Format
10019-651
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
sevoflurane (source: ndc)
Generic Name
sevoflurane (source: ndc)
Application Number
ANDA075895 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mL/250mL
Packaging
- 6 BOTTLE in 1 CARTON (10019-651-64) / 250 mL in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "51e533f0-ea5a-4210-8fa9-11c1897093a6", "openfda": {"nui": ["N0000175975", "N0000175681"], "upc": ["0310019651644"], "unii": ["38LVP0K73A"], "rxcui": ["200243"], "spl_set_id": ["ea8bf997-2c71-4014-b18d-4f7ab45dfa19"], "pharm_class_pe": ["General Anesthesia [PE]"], "pharm_class_epc": ["General Anesthetic [EPC]"], "manufacturer_name": ["Baxter Healthcare Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 BOTTLE in 1 CARTON (10019-651-64) / 250 mL in 1 BOTTLE", "package_ndc": "10019-651-64", "marketing_start_date": "20020702"}], "brand_name": "Sevoflurane", "product_id": "10019-651_51e533f0-ea5a-4210-8fa9-11c1897093a6", "dosage_form": "LIQUID", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "10019-651", "generic_name": "Sevoflurane", "labeler_name": "Baxter Healthcare Company", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sevoflurane", "active_ingredients": [{"name": "SEVOFLURANE", "strength": "250 mL/250mL"}], "application_number": "ANDA075895", "marketing_category": "ANDA", "marketing_start_date": "20020702", "listing_expiration_date": "20271231"}