NDC 83301-0070-01 - Sevoflurane, (Volatile for Inhalation)

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
83301-0070
Requested NDC
83301-0070-01
Package NDCs from labels
83301-0070-1, 83301-0070-01
Manufacturer
Mullan Pharmaceutical Inc. | Shandong New Time Pharmaceutical Co. Ltd.
Effective date
2026-03-23
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Sevoflurane USP volatile liquid for inhalationMullan Pharmaceutical Inc. | Shandong New Time Pharmaceutical Co. Ltd.2026-03-23HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83301-0070-1Sevoflurane, (Volatile for Inhalation)1 in 1 CARTONLIQUID13
83301-0070-1Sevoflurane, (Volatile for Inhalation)250 mL in 1 BOTTLE, GLASSLIQUID2503

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
83301-0070-1ML - Milliliter83301-00700264ec4e-910e-4d55-89b2-58061c5deb3112026-02-05

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 13 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SevofluraneSEVOFLURANEShandong New Time Pharmaceutical Co., Ltd.c808afe1-ebf1-44cf-9187-09656331bff52026-06-02Warnings, Adverse reactionsExact identifier
application number: ANDA214382
rxcui: 200243
unii: 38LVP0K73A
Sevoflurane, (Volatile for Inhalation)SEVOFLURANEMullan Pharmaceutical Inc.0ca6da3a-6a18-400d-8c49-08a5534b025f2026-03-23Warnings, Adverse reactionsExact identifier
application number: ANDA214382
ndc (package): 83301-0070-1
ndc (product): 83301-0070
ndc11 (package): 83301007001
rxcui: 200243
spl id: 4db52cc7-3ca6-0aaf-e063-6294a90a0dc1
spl set id: 0ca6da3a-6a18-400d-8c49-08a5534b025f
unii: 38LVP0K73A
SevofluraneSEVOFLURANEHalocarbon Life Sciences, LLCbdde7502-6218-401c-9a4f-dd3bc3a80f722025-12-18Warnings, Adverse reactionsExact identifier
rxcui: 200243
unii: 38LVP0K73A
SojournSEVOFLURANEPiramal Critical Care Incfedfd1db-7e32-44b2-89e9-7bb00ee6810d2025-12-01Warnings, Adverse reactionsExact identifier
rxcui: 200243
unii: 38LVP0K73A
SevofluraneSEVOFLURANEPiramal Critical Care Incb23e14d7-9e5b-13f4-e053-2a95a90a0cde2025-12-01Warnings, Adverse reactionsExact identifier
rxcui: 200243
unii: 38LVP0K73A
SevofluraneSEVOFLURANEBryant Ranch Prepack06b9f724-6425-4976-93eb-b9ca343ef5cf2025-11-06Warnings, Adverse reactionsExact identifier
rxcui: 200243
unii: 38LVP0K73A
SevofluraneSEVOFLURANEPiramal Critical Care Inc3dbab949-6ab7-4040-9c81-314e5bb61d412025-10-03Warnings, Adverse reactionsExact identifier
rxcui: 200243
unii: 38LVP0K73A
SEVOFLURANESEVOFLURANEBaxter Healthcare Corporation22700993-851a-48aa-941e-1d2b6b04081f2025-04-30Warnings, Adverse reactionsExact identifier
rxcui: 200243
unii: 38LVP0K73A
SevofluraneSEVOFLURANEBaxter Healthcare Companyea8bf997-2c71-4014-b18d-4f7ab45dfa192025-03-28Warnings, Adverse reactionsExact identifier
rxcui: 200243
unii: 38LVP0K73A
UltaneSEVOFLURANEAbbVie Inc.c9aa6489-5a36-44ed-9512-b996833d82f72025-02-12Warnings, Adverse reactionsExact identifier
rxcui: 200243
unii: 38LVP0K73A
UltaneSEVOFLURANEAbbVie Inc.4c6e76bc-c964-4955-e0a3-511d3386a9cc2025-01-13Warnings, Adverse reactionsExact identifier
rxcui: 200243
unii: 38LVP0K73A
SevofluraneSEVOFLURANELannett Company, Inc.5bfc1cef-824d-4ebf-bb4d-fbc46c0abb792023-09-19Warnings, Adverse reactionsExact identifier
application number: ANDA214382
rxcui: 200243
unii: 38LVP0K73A
SevofluraneSEVOFLURANESandoz Inc.8604f245-fa99-4092-9042-058aa42e0b742022-11-08Warnings, Adverse reactionsExact identifier
rxcui: 200243
unii: 38LVP0K73A

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.