NDC 0338-0149 - Plasma-Lyte 148 and dextrose

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
0338-0149
Package NDCs from labels
0338-0149-03, 0338-0149-04
Manufacturer
Baxter Healthcare Corporation
Effective date
2006-04-13
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Plasma-Lyte 148 and dextrose - Baxter Healthcare CorporationBaxter Healthcare Corporation2006-04-13HUMAN PRESCRIPTION DRUG LABELING

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Dextrose hydrousACTIVE INGREDIENTLX22YL083GPLASMA-LYTE 148 AND DEXTROSE (SODIUM CHLORIDE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, SODIUM GLUCONATE, SODIUM ACETATE AND DEXTROSE) INJECTION, SOLUTION [BAXTER HEALTHCARE CORPORATION]1
Magnesium ChlorideACTIVE INGREDIENT02F3473H9OPLASMA-LYTE 148 AND DEXTROSE (SODIUM CHLORIDE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, SODIUM GLUCONATE, SODIUM ACETATE AND DEXTROSE) INJECTION, SOLUTION [BAXTER HEALTHCARE CORPORATION]1
Potassium ChlorideACTIVE INGREDIENT660YQ98I10PLASMA-LYTE 148 AND DEXTROSE (SODIUM CHLORIDE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, SODIUM GLUCONATE, SODIUM ACETATE AND DEXTROSE) INJECTION, SOLUTION [BAXTER HEALTHCARE CORPORATION]1
Sodium AcetateACTIVE INGREDIENT4550K0SC9BPLASMA-LYTE 148 AND DEXTROSE (SODIUM CHLORIDE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, SODIUM GLUCONATE, SODIUM ACETATE AND DEXTROSE) INJECTION, SOLUTION [BAXTER HEALTHCARE CORPORATION]1
Sodium ChlorideACTIVE INGREDIENT451W47IQ8XPLASMA-LYTE 148 AND DEXTROSE (SODIUM CHLORIDE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, SODIUM GLUCONATE, SODIUM ACETATE AND DEXTROSE) INJECTION, SOLUTION [BAXTER HEALTHCARE CORPORATION]1
Sodium GluconateACTIVE INGREDIENTR6Q3791S76PLASMA-LYTE 148 AND DEXTROSE (SODIUM CHLORIDE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, SODIUM GLUCONATE, SODIUM ACETATE AND DEXTROSE) INJECTION, SOLUTION [BAXTER HEALTHCARE CORPORATION]1
dextroseACTIVE MOIETYIY9XDZ35W2PLASMA-LYTE 148 AND DEXTROSE (SODIUM CHLORIDE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, SODIUM GLUCONATE, SODIUM ACETATE AND DEXTROSE) INJECTION, SOLUTION [BAXTER HEALTHCARE CORPORATION]1
Magnesium ChlorideACTIVE MOIETY02F3473H9OPLASMA-LYTE 148 AND DEXTROSE (SODIUM CHLORIDE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, SODIUM GLUCONATE, SODIUM ACETATE AND DEXTROSE) INJECTION, SOLUTION [BAXTER HEALTHCARE CORPORATION]1
Potassium ChlorideACTIVE MOIETY660YQ98I10PLASMA-LYTE 148 AND DEXTROSE (SODIUM CHLORIDE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, SODIUM GLUCONATE, SODIUM ACETATE AND DEXTROSE) INJECTION, SOLUTION [BAXTER HEALTHCARE CORPORATION]1
sodium acetateACTIVE MOIETY4550K0SC9BPLASMA-LYTE 148 AND DEXTROSE (SODIUM CHLORIDE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, SODIUM GLUCONATE, SODIUM ACETATE AND DEXTROSE) INJECTION, SOLUTION [BAXTER HEALTHCARE CORPORATION]1
Sodium ChlorideACTIVE MOIETY451W47IQ8XPLASMA-LYTE 148 AND DEXTROSE (SODIUM CHLORIDE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, SODIUM GLUCONATE, SODIUM ACETATE AND DEXTROSE) INJECTION, SOLUTION [BAXTER HEALTHCARE CORPORATION]1
sodium gluconateACTIVE MOIETYR6Q3791S76PLASMA-LYTE 148 AND DEXTROSE (SODIUM CHLORIDE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, SODIUM GLUCONATE, SODIUM ACETATE AND DEXTROSE) INJECTION, SOLUTION [BAXTER HEALTHCARE CORPORATION]1
Hydrochloric acidINACTIVE INGREDIENTQTT17582CBPLASMA-LYTE 148 AND DEXTROSE (SODIUM CHLORIDE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, SODIUM GLUCONATE, SODIUM ACETATE AND DEXTROSE) INJECTION, SOLUTION [BAXTER HEALTHCARE CORPORATION]1
WaterINACTIVE INGREDIENT059QF0KO0RPLASMA-LYTE 148 AND DEXTROSE (SODIUM CHLORIDE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, SODIUM GLUCONATE, SODIUM ACETATE AND DEXTROSE) INJECTION, SOLUTION [BAXTER HEALTHCARE CORPORATION]1

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 ยท 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
81d75979-e503-486b-ae76-5f11252e694d81d75979-e503-486b-ae76-5f11252e694d2006-04-13Warnings, Adverse reactionsExact identifier
spl id: 81d75979-e503-486b-ae76-5f11252e694d
spl set id: 81d75979-e503-486b-ae76-5f11252e694d

Reported adverse events (FAERS/openFDA)#

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