sevoflurane
Generic: sevoflurane
Labeler: sandoz inc.Drug Facts
Product Profile
Brand Name
sevoflurane
Generic Name
sevoflurane
Labeler
sandoz inc.
Dosage Form
LIQUID
Routes
Active Ingredients
sevoflurane 250 mL/250mL
Manufacturer
Identifiers & Regulatory
Product NDC
0781-6160
Product ID
0781-6160_ecf89ead-16b2-91cf-e053-2995a90adc93
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203793
Listing Expiration
2026-12-31
Marketing Start
2017-01-25
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
07816160
Hyphenated Format
0781-6160
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
ANDA203793 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mL/250mL
Packaging
- 6 BOTTLE, GLASS in 1 CARTON (0781-6160-86) / 250 mL in 1 BOTTLE, GLASS (0781-6160-43)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "ecf89ead-16b2-91cf-e053-2995a90adc93", "openfda": {"nui": ["N0000175975", "N0000175681"], "upc": ["0307816160431"], "unii": ["38LVP0K73A"], "rxcui": ["200243"], "spl_set_id": ["8604f245-fa99-4092-9042-058aa42e0b74"], "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 (0781-6160-86) / 250 mL in 1 BOTTLE, GLASS (0781-6160-43)", "package_ndc": "0781-6160-86", "marketing_start_date": "20170125"}], "brand_name": "Sevoflurane", "product_id": "0781-6160_ecf89ead-16b2-91cf-e053-2995a90adc93", "dosage_form": "LIQUID", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "0781-6160", "generic_name": "Sevoflurane", "labeler_name": "Sandoz Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sevoflurane", "active_ingredients": [{"name": "SEVOFLURANE", "strength": "250 mL/250mL"}], "application_number": "ANDA203793", "marketing_category": "ANDA", "marketing_start_date": "20170125", "listing_expiration_date": "20261231"}