FDA.reportPublic FDA data

NDC 51672-3019-3 - Sodium Chloride

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
51672-3019
Requested NDC
51672-3019-3
Package NDCs from labels
51672-3019-5, 51672-3019-3
Manufacturer
Taro Pharmaceuticals U.S.A., Inc.
Effective date
2008-02-08
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Sodium Chloride Injection USP, 0.9%Taro Pharmaceuticals U.S.A., Inc.2008-02-08HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51672-3019-3Sodium Chloride10 mL in 1 AMPULEINJECTION, SOLUTION101
51672-3019-3Sodium Chloride20 in 1 CARTONINJECTION, SOLUTION201
51672-3019-5Sodium Chloride20 in 1 CARTONINJECTION, SOLUTION201
51672-3019-5Sodium Chloride5 mL in 1 AMPULEINJECTION, SOLUTION51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51672-3019SODIUM CHLORIDE (SODIUM CHLORIDE) INJECTION, SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.]14 package rows20080215_CF16BFB8-CD72-49E7-B74F-C99292CAB53B.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Sodium ChlorideACTIVE INGREDIENT451W47IQ8XSODIUM CHLORIDE (SODIUM CHLORIDE) INJECTION, SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.]1
Sodium ChlorideACTIVE MOIETY451W47IQ8XSODIUM CHLORIDE (SODIUM CHLORIDE) INJECTION, SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.]1
hydrochloric acidINACTIVE INGREDIENTQTT17582CBSODIUM CHLORIDE (SODIUM CHLORIDE) INJECTION, SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.]1
sodium hydroxideINACTIVE INGREDIENT55X04QC32ISODIUM CHLORIDE (SODIUM CHLORIDE) INJECTION, SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.]1
waterINACTIVE INGREDIENT059QF0KO0RSODIUM CHLORIDE (SODIUM CHLORIDE) INJECTION, SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.]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 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Sodium ChlorideSODIUM CHLORIDEHospira, Inc.8eb172da-dcd4-4660-4a8f-ad44a14b4af72024-11-06Adverse reactionsExact identifier
rxcui: 1807628
4D2A3123-168B-CF28-07A6-D395DC4C8945CF16BFB8-CD72-49E7-B74F-C99292CAB53B2008-02-08Adverse reactionsExact identifier
spl id: 4D2A3123-168B-CF28-07A6-D395DC4C8945
spl set id: CF16BFB8-CD72-49E7-B74F-C99292CAB53B

Reported adverse events (FAERS/openFDA)#

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