sevoflurane
Generic: sevoflurane
Labeler: baxter healthcare corporationDrug Facts
Product Profile
Brand Name
sevoflurane
Generic Name
sevoflurane
Labeler
baxter healthcare corporation
Dosage Form
LIQUID
Routes
Active Ingredients
sevoflurane 250 mL/250mL
Manufacturer
Identifiers & Regulatory
Product NDC
10019-653
Product ID
10019-653_e04090f9-97a3-4fe5-9bc1-c4a86ac9a6a1
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA075895
Listing Expiration
2027-12-31
Marketing Start
2002-07-07
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
10019653
Hyphenated Format
10019-653
Supplemental Identifiers
RxCUI
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 (10019-653-64) / 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": "e04090f9-97a3-4fe5-9bc1-c4a86ac9a6a1", "openfda": {"nui": ["N0000175975", "N0000175681"], "unii": ["38LVP0K73A"], "rxcui": ["200243"], "spl_set_id": ["22700993-851a-48aa-941e-1d2b6b04081f"], "pharm_class_pe": ["General Anesthesia [PE]"], "pharm_class_epc": ["General Anesthetic [EPC]"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 BOTTLE in 1 CARTON (10019-653-64) / 250 mL in 1 BOTTLE", "package_ndc": "10019-653-64", "marketing_start_date": "20020707"}], "brand_name": "SEVOFLURANE", "product_id": "10019-653_e04090f9-97a3-4fe5-9bc1-c4a86ac9a6a1", "dosage_form": "LIQUID", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "10019-653", "generic_name": "Sevoflurane", "labeler_name": "Baxter Healthcare Corporation", "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": "20020707", "listing_expiration_date": "20271231"}