FDA.reportPublic FDA data

NDC 42023-221-01 - ERTAPENEM

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
42023-221
Requested NDC
42023-221-01
Package NDCs from labels
42023-221-89, 42023-221-85, 42023-221-01, 42023-221-10
Manufacturer
ENDO USA, Inc. | Merck Sharp & Dohme LLC
Effective date
2026-03-02
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
ERTAPENEM - ENDO USA, Inc. | Merck Sharp & Dohme LLCENDO USA, Inc. | Merck Sharp & Dohme LLC2026-03-02HUMAN PRESCRIPTION DRUG LABEL
ERTAPENEM - ENDO USA, Inc. | Merck Sharp & Dohme LLCENDO USA, Inc. | Merck Sharp & Dohme LLC2026-03-02HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
42023-221-01ERTAPENEM1 in 1 VIAL, SINGLE-DOSEINJECTION, POWDER, LYOPHILIZED,113
42023-221-10ERTAPENEM10 in 1 PACKAGEINJECTION, POWDER, LYOPHILIZED,1013
42023-221-85ERTAPENEM10 in 1 PACKAGEINJECTION, POWDER, LYOPHILIZED,1013
42023-221-89ERTAPENEM1 in 1 VIAL, SINGLE-DOSEINJECTION, POWDER, LYOPHILIZED,113

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
42023-221ERTAPENEM (ERTAPENEM SODIUM) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [ENDO USA, INC.]10Current NDC, Legacy NDC, 2 package rows20240716_657855f2-7c92-4aa8-9c3d-51d08e56a09a.zip
42023-221ERTAPENEM (ERTAPENEM SODIUM) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [ENDO USA, INC.]9Current NDC, Legacy NDC, 2 package rows20240716_41304b1d-7db4-468a-ab1d-04e56fb50de4.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
42023-221-01EA - Each42023-221ab48327d-4a9d-49ae-93cb-36b2e50be6f212018-08-13
42023-221-10EA - Each42023-2215bce14c2-8926-4eb4-a8cc-2bba14d9ebd912018-08-13
42023-221-85EA - Each42023-221cca54412-b1b8-4749-9c80-0c30149b3ec612018-12-13
42023-221-89EA - Each42023-221014f44b1-2664-42fc-bdd2-c33f5769861b12018-12-13

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 7 of 12 · 222 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Alka-Seltzer Heartburn Relief Lemon LimeANHYDROUS CITRIC ACID, SODIUM BICARBONATE (HEAT-TREATED)Bayer Healthcare LLCcc21af24-9a5b-6831-e053-2a95a90a0af42025-04-01WarningsExact identifier
unii: 8MDF5V39QO
Alka-Seltzer Heartburn Relief Extra StrengthANHYDROUS CITRIC ACID, SODIUM BICARBONATE (HEAT-TREATED)Bayer Healthcare LLCdc1641f8-54c2-0d86-e053-2995a90a1dce2025-03-11WarningsExact identifier
unii: 8MDF5V39QO
Acid Reducer PowderOMEPRAZOLE AND SODIUM BICARBONATEDr. Reddy's Laboratories Inc.,6f8452f8-8c2c-6700-a11d-1531023056c52025-03-03WarningsExact identifier
unii: 8MDF5V39QO
Well at WalgreensSODIUM BICARBONATE, SODIUM CHLORIDEWalgreen Companycb5d3d9d-2481-4303-b6af-0002de8c90652025-01-31WarningsExact identifier
unii: 8MDF5V39QO
Sinus Wash PacketSODIUM BICARBONATE, SODIUM CHLORIDERITE AID CORPORATIONd5b44ae7-81e8-1413-e053-2995a90a59332025-01-31WarningsExact identifier
unii: 8MDF5V39QO
Sinus Wash Saline Refills MeijerSODIUM BICARBONATE, SODIUM CHLORIDEMeijer, Inc.dd7465fe-503a-4e34-e053-2995a90a27782025-01-31WarningsExact identifier
unii: 8MDF5V39QO
SinuCleanseSODIUM BICARBONATE, SODIUM CHLORIDEASCENT CONSUMER PRODUCTS, INC.ff4df6c5-c85f-406a-89d7-8c2853fd5e102025-01-31WarningsExact identifier
unii: 8MDF5V39QO
CVSSODIUM BICARBONATE, SODIUM CHLORIDECVS Pharmacybccefef8-f92d-42fc-90fc-86644d1df6552025-01-31WarningsExact identifier
unii: 8MDF5V39QO
Well at WalgreensSODIUM BICARBONATE, SODIUM CHLORIDEWalgreen Companybcd336b4-9189-44d5-ae6d-81e535eff6b52025-01-31WarningsExact identifier
unii: 8MDF5V39QO
SinuCleanseSODIUM BICARBONATE, SODIUM CHLORIDEASCENT CONSUMER PRODUCTS, INC.c33bf872-54aa-45e0-9e40-a6565a13f1982025-01-31WarningsExact identifier
unii: 8MDF5V39QO
Sodium Bicarbonate 10 gr (650 mg)SODIUM BICARBONATECitraGen Pharmaceuticals Inc.650fa284-5829-588f-e053-2991aa0a9a0e2025-01-30WarningsExact identifier
unii: 8MDF5V39QO
Sodium Bicarbonate 5 gr (325 mg)SODIUM BICARBONATECitraGen Pharmaceuticals Inc.68aadbd9-f1c6-8a23-e053-2991aa0afd962025-01-30WarningsExact identifier
unii: 8MDF5V39QO
Sodium BicarbonateSODIUM BICARBONATEWorld Perfumes Inca83544e4-ec09-1e95-e053-2995a90ab7b92025-01-15WarningsExact identifier
unii: 8MDF5V39QO
Sodium Bicarbonate 10 grSODIUM BICARBONATEReliable 1 Laboratories LLC321a772c-c44c-3d4e-e054-00144ff8d46c2025-01-15WarningsExact identifier
unii: 8MDF5V39QO
Premixed saline packetsSODIUM CHLORIDE, SODIUM BICARBONATEShenzhen Kerui lntl Trading Co., Ltd0d11e07b-c137-6efc-e063-6394a90a6bba2025-01-09WarningsExact identifier
unii: 8MDF5V39QO
Caring Mill Bug Bite Relief WipesCARING MILL BUG BITE RELIEF WIPESShenzhen Shierjie Biological Engineering Co., LTD2a373589-aec3-b294-e063-6394a90a39f12025-01-08WarningsExact identifier
unii: 8MDF5V39QO
SODIUM BICARBONATESODIUM BICARBONATEHF Acquisition Co LLC, DBA HealthFirst9545d58c-1c49-79b3-e053-2995a90a9d402025-01-08Warnings, Adverse reactionsExact identifier
unii: 8MDF5V39QO
7.5% SODIUM BICARBONATE7.5% SODIUM BICARBONATEHF Acquisition Co LLC, DBA HealthFirst9d4bbd21-f59c-7e9c-e053-2a95a90a08262025-01-08Warnings, Adverse reactionsExact identifier
unii: 8MDF5V39QO
EcoDent Ultimate Essential Mouthcare Sparkling Clean MintSODIUM BICARBONATELotus Brands, Inc.4a95c8c1-db7c-4791-ac58-3eac216a01262024-12-18WarningsExact identifier
unii: 8MDF5V39QO
EcoDent Ultimate Essential Mouthcare Spicy-Cool CinnamonSODIUM BICARBONATELotus Brands, Inc.6703b29d-cdc9-4c74-91c0-fb0c98dd043e2024-12-18WarningsExact identifier
unii: 8MDF5V39QO

Reported adverse events (FAERS/openFDA)#

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