FDA.reportPublic FDA data

DEXTROSE

Product NDC
51662-1380
11-digit product format
516621380
Labeler code
51662
Product ID
51662-1380_ef7bd5a0-02ac-7b66-e053-2995a90a8ffa
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
DEXTROSE
Dosage form
INJECTION
Route
PARENTERAL
Labeler
HF Acquisition Co LLC, DBA HealthFirst
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2019-10-29
Marketing end
0000-00-00
Substance
DEXTROSE MONOHYDRATE
Active strength
500 mg/mL
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct51662-1380IInactivated by FDA2026-10-05
excluded packagepackage51662-138051662-1380-1IInactivated by FDA2026-10-05

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 4 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproductd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage51662-1380-1d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded productproductf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage51662-1380-1f5e01cc5f278…a2eaf40c39c3…

Reported adverse events (FAERS/openFDA)#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
cb89b86a-369e-4204-8910-ae797c503af3Product name120230706
d4880ace-a516-8c47-8dfd-73a4ba5887d7Product name220180830
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51662-1380-1DEXTROSE1 in 1 CARTONINJECTION15
51662-1380-1DEXTROSE50 mL in 1 SYRINGEINJECTION505

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51662-1380DEXTROSE INJECTION [HF ACQUISITION CO LLC, DBA HEALTHFIRST]5Legacy NDC, 2 package rows20221211_96110249-e7c2-b7f5-e053-2a95a90a0d06.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
727517dextrose 50 % in 50 ML Prefilled SyringePSN96110249-e7c2-b7f5-e053-2a95a90a0d065
72751750 ML glucose 500 MG/ML Prefilled SyringeSCD96110249-e7c2-b7f5-e053-2a95a90a0d065
72751750 ML dextrose 50 % Prefilled SyringeSY96110249-e7c2-b7f5-e053-2a95a90a0d065
727517dextrose 25 GM per 50 ML Prefilled SyringeSY96110249-e7c2-b7f5-e053-2a95a90a0d065

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
51662-1380-1516621380011 SYRINGE in 1 CARTON (51662-1380-1) > 50 mL in 1 SYRINGE1 syringe2019-10-290000-00-00NoNoCurrent