sevoflurane
Generic: sevoflurane
Labeler: lannett company, inc.Drug Facts
Product Profile
Brand Name
sevoflurane
Generic Name
sevoflurane
Labeler
lannett company, inc.
Dosage Form
LIQUID
Routes
Active Ingredients
sevoflurane 250 mL/250mL
Manufacturer
Identifiers & Regulatory
Product NDC
0527-6123
Product ID
0527-6123_f3d34dea-e901-46b9-80f8-b314ca57020c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA214382
Listing Expiration
2026-12-31
Marketing Start
2023-08-18
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
05276123
Hyphenated Format
0527-6123
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
ANDA214382 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mL/250mL
Packaging
- 1 BOTTLE, GLASS in 1 CARTON (0527-6123-74) / 250 mL in 1 BOTTLE, GLASS
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "f3d34dea-e901-46b9-80f8-b314ca57020c", "openfda": {"nui": ["N0000175975", "N0000175681"], "unii": ["38LVP0K73A"], "rxcui": ["200243"], "spl_set_id": ["5bfc1cef-824d-4ebf-bb4d-fbc46c0abb79"], "pharm_class_pe": ["General Anesthesia [PE]"], "pharm_class_epc": ["General Anesthetic [EPC]"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, GLASS in 1 CARTON (0527-6123-74) / 250 mL in 1 BOTTLE, GLASS", "package_ndc": "0527-6123-74", "marketing_start_date": "20230818"}], "brand_name": "Sevoflurane", "product_id": "0527-6123_f3d34dea-e901-46b9-80f8-b314ca57020c", "dosage_form": "LIQUID", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "0527-6123", "generic_name": "Sevoflurane", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sevoflurane", "active_ingredients": [{"name": "SEVOFLURANE", "strength": "250 mL/250mL"}], "application_number": "ANDA214382", "marketing_category": "ANDA", "marketing_start_date": "20230818", "listing_expiration_date": "20261231"}