FDA.reportPublic FDA data

NDC 72572-747-01 - Sterile Water

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
72572-747
Requested NDC
72572-747-01
Package NDCs from labels
72572-747-01, 72572-747-10
Manufacturer
Civica, Inc. | Hikma Pharmaceuticals USA Inc.
Effective date
2023-04-07
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Sterile Water for Injection, USPCivica, Inc. | Hikma Pharmaceuticals USA Inc.2023-04-07HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72572-747-01Sterile Water10 mL in 1 VIALINJECTION, SOLUTION104
72572-747-10Sterile Water10 in 1 CARTONINJECTION, SOLUTION104

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72572-747STERILE WATER (WATER) INJECTION, SOLUTION [CIVICA, INC.]4Current NDC, Legacy NDC, 2 package rows20230413_3f49eedf-5bf5-4a95-b704-c956d860ca04.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72572-747-01ML - Milliliter72572-7476eae8b0f-134e-4f91-9441-20b9bc19e32912022-08-04
72572-747-10ML - Milliliter72572-7472c1bebb5-206a-4f04-804c-1bee340291e012022-08-04

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 9 of 9 · 161 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Sterile WaterWATERBaxter Healthcare Company210dc9ab-d6ca-4552-ac19-1be17792d2902016-05-31Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R

Reported adverse events (FAERS/openFDA)#

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