FDA.reportPublic FDA data

NDC 0006-3061-01 - EMEND

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
0006-3061
Requested NDC
0006-3061-01
Package NDCs from labels
0006-3061-01, 0006-3061-00, 0006-3061-03, 0006-3061-02, 0006-3061-04
Manufacturer
Merck Sharp & Dohme LLC
Effective date
2026-02-20
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
EMEND - Merck Sharp & Dohme LLCMerck Sharp & Dohme LLC2026-02-20HUMAN PRESCRIPTION DRUG LABEL
EMEND - Merck Sharp & Dohme Corp.Merck Sharp & Dohme Corp.2020-06-26HUMAN PRESCRIPTION DRUG LABEL
EMEND - Merck Sharp & Dohme Corp.Merck Sharp & Dohme Corp.2020-04-30HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0006-3061-00EMEND1 in 1 CARTONINJECTION, POWDER, LYOPHILIZED,120
0006-3061-01EMEND5 mL in 1 VIAL, SINGLE-DOSEINJECTION, POWDER, LYOPHILIZED,520

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0006-3061EMEND (FOSAPREPITANT DIMEGLUMINE) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [MERCK SHARP & DOHME LLC]18Current NDC, Legacy NDC, 2 package rows20240111_8d66803a-6811-4c29-9c57-e16acfa87f21.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0006-3061-00EA - Each0006-3061136fbe9b-7f31-4ce1-acb2-16d66d0c0bc712017-07-07
0006-3061-01EA - Each0006-3061bc8e7553-f2ce-4c6e-ab40-829bbeb9fddd12018-03-08
0006-3061-02EA - Each0006-30616734df7f-a0c7-4344-9a9a-887329f5586d12019-08-06
0006-3061-03EA - Each0006-3061c4d6bb40-a295-48c8-bba4-3889616b3aff12020-07-13
0006-3061-04EA - Each0006-3061585908e3-6134-4f36-84c6-2d2e17be473012019-07-02

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 4 · 70 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
FosaprepitantFOSAPREPITANT DIMEGLUMINEBluePoint Laboratories2d30d839-bb88-46ce-a9ed-66fe32a12a7a2026-09-02Warnings, Adverse reactionsExact identifier
rxcui: 1731077
unii: D35FM8T64X
Rohto Max StrengthNAPHAZOLINE HYDROCHLORIDE, POLYSORBATE 80The Mentholatum Companye4b49550-1ca3-4bd7-854d-409b53fa5e262026-08-20WarningsExact identifier
unii: 6OZP39ZG8H
fosaprepitantFOSAPREPITANTMylan Institutional LLC9b6d5ea3-2f7a-4501-9a4a-6fa1a7c2d50a2026-08-15Warnings, Adverse reactionsExact identifier
rxcui: 1731077
unii: D35FM8T64X
FosaprepitantFOSAPREPITANT DIMEGLUMINECamber Pharmaceuticals, Inc.7dbdf8f5-6936-4143-b52d-96774b799a7d2026-08-11Warnings, Adverse reactionsExact identifier
rxcui: 1731077
unii: D35FM8T64X
NAVITRUXFOSAPREPITANTAVYXA Pharma, LLCa41b7c3a-1376-43a7-b5b9-6ba2eba1e1692026-07-29Warnings, Adverse reactionsExact identifier
rxcui: 1731077
unii: D35FM8T64X
Droptics Dry Eye ReliefCARBOXYMETHYLCELLULOSE SODIUM,GLYCERIN,POLYSORBATE 80Droptics LLC29d7614b-f4b7-48e2-97c5-d1bff27731d22026-07-22WarningsExact identifier
unii: 6OZP39ZG8H
FosaprepitantFOSAPREPITANTNorthstar Rx LLCbf207918-100d-4917-88b0-3433c0e722492026-07-09Warnings, Adverse reactionsExact identifier
rxcui: 1731077
unii: D35FM8T64X
Rohto Cool ReliefNAPHAZOLINE HYDROCHLORIDE, POLYSORBATE 80The Mentholatum Companydc8f1ff3-87ae-47ca-815f-5a0e34f8cf302026-06-19WarningsExact identifier
unii: 6OZP39ZG8H
BM BM182 DROPSHEPAR SULF, GRAPHITES, MERC SOL, MURIATIC ACIDTotal Operations Management LLC DBA:Bestmade Natural Products Micro5423bde6-3e31-38b0-e063-6294a90afb2d2026-06-13WarningsExact identifier
unii: QTT17582CB
BM BM182 DROPSHEPAR SULF, GRAPHITES, MERC SOL, MURIATIC ACIDBM Private Limited540d11e3-e4a1-0ca2-e063-6394a90a3c262026-06-12WarningsExact identifier
unii: QTT17582CB
FosaprepitantFOSAPREPITANT DIMEGLUMINEBaxter Healthcare Corporation3ed3e0a9-a0a8-4555-9f73-2043e79e33982026-05-29Warnings, Adverse reactionsExact identifier
rxcui: 1731077
unii: D35FM8T64X
Muriaticum acidumHYDROCHLORIC ACIDBoiron8643bc58-bb0e-5c79-e053-2991aa0a02ae2026-05-19WarningsExact identifier
unii: QTT17582CB
FosaprepitantFOSAPREPITANTBryant Ranch Prepack679c195a-cf59-4ca5-aa05-fa35d08ddb5c2026-05-06Warnings, Adverse reactionsExact identifier
rxcui: 1731077
unii: D35FM8T64X
FOSAPREPITANT DIMEGLUMINEFOSAPREPITANT DIMEGLUMINEEugia US LLC19919480-960b-4741-9611-c133d68512f52026-04-01Warnings, Adverse reactionsExact identifier
rxcui: 1731077
unii: D35FM8T64X
FOCINVEZFOSAPREPITANT DIMEGLUMINESteriscience Specialties Private Limited18a60093-cec8-1b8c-e063-6394a90a89022026-03-30Warnings, Adverse reactionsExact identifier
unii: D35FM8T64X
FOSAPREPITANT DIMEGLUMINEFOSAPREPITANT DIMEGLUMINEHikma Pharmaceuticals USA Inc.1a7d2f44-b578-4d99-a4ff-f267626064d02026-03-19Warnings, Adverse reactionsExact identifier
rxcui: 1731077
unii: D35FM8T64X
FOSAPREPITANT DIMEGLUMINEFOSAPREPITANT DIMEGLUMINEHikma Pharmaceuticals USA Inc.1cc7d482-5d45-4621-9ffc-cd3f7c54614d2026-03-19Warnings, Adverse reactionsExact identifier
rxcui: 1731077
unii: D35FM8T64X
Skin Irritations and Itch ReliefAGARICUS MUSCARIUS, ALUMINA, ANAGALLIS ARVENSIS, ANTIMONIUM TARTARICUM, APIS MELLIFICA, ARSENICUM ALBUM, ARSENICUM IODATUM, BOVISTA, CAUSTICUM, DOLICHOS PRURIENS, FAGOPYRUM ESCULENTUM, GRAPHITES, KALI MURIATICUM, MURIATICUM ACIDUM, OLEANDER, PETROLEUM, PIX LIQUIDA, RADIUM BROMATUM (12X, 30X, 1LM), RHUS TOX, SELENIUM METALLICUM, SULPHUR AND URTICA URENS.King Bio Inc.d139d2f1-0369-4963-9f3d-c4cc0f1ea2dd2026-03-10WarningsExact identifier
unii: QTT17582CB
Refresh Optive Mega-3 PFCARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN, POLYSORBATE 80Allergan, Inc.326cb5d6-c784-404f-9a13-6d69262dda6e2026-03-01WarningsExact identifier
unii: 6OZP39ZG8H
EMENDFOSAPREPITANT DIMEGLUMINEMerck Sharp & Dohme LLC8d66803a-6811-4c29-9c57-e16acfa87f212026-02-20Warnings, Adverse reactionsExact identifier
application number: NDA022023
ndc (package): 0006-3061-01
ndc (package): 0006-3061-00
ndc (product): 0006-3061
ndc11 (package): 00006306101
rxcui: 1731082
rxcui: 1731077
spl id: 20906e8e-8a3e-4c45-a657-6d4c1945af09
spl set id: 8d66803a-6811-4c29-9c57-e16acfa87f21
unii: D35FM8T64X

Reported adverse events (FAERS/openFDA)#

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