FDA.reportPublic FDA data

NDC 0093-9044 - PEG-3350, SODIUM SULFATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE, SODIUM ASCORBATE AND ASCORBIC ACID

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
0093-9044
Package NDCs from labels
0093-9044-19
Manufacturer
Teva Pharmaceuticals USA, Inc. | Novel Laboratories, Inc.
Effective date
2022-04-14
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
POUCH A - Teva Pharmaceuticals USA, Inc. | Novel Laboratories, Inc.Teva Pharmaceuticals USA, Inc. | Novel Laboratories, Inc.2022-04-14HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0093-9044-19PEG-3350, SODIUM SULFATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE, SODIUM ASCORBATE AND ASCORBIC ACID1 L in 1 POUCHPOWDER, FOR SOLUTION1 L7.5 g in 1L3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0093-9044PEG-3350, SODIUM SULFATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE, SODIUM ASCORBATE AND ASCORBIC ACID (PEG-3350, SODIUM SULFATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE, SODIUM ASCORBATE AND ASCORBIC ACID) KIT [TEVA PHARMACEUTICALS USA, INC.]3Unmatched20230223_475a06c6-f295-406c-a110-f1497cf51566.zip