NDC 51044-101 - Cupric Sulfate Pentahydrate

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: 51044-101
Package NDCs from labels: 51044-101-25
Manufacturer: Fondel Chemicals Ltd.
Effective date: 2010-06-25
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Cupric Sulfate Pentahydrate Label	Fondel Chemicals Ltd.	2010-06-25	OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
51044-101-25	Cupric Sulfate Pentahydrate	25 kg in 1 BAG	POWDER, FOR SOLUTION	25		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51044-101	CUPRIC SULFATE PENTAHYDRATE (CUPRIC SULFATE) POWDER, FOR SOLUTION [FONDEL CHEMICALS LTD.]	4	1 package rows	20100628_74fae9fa-4ee5-4586-925f-1f8b0a8bded8.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
Cupric Sulfate	ACTIVE INGREDIENT	LRX7AJ16DT	CUPRIC SULFATE PENTAHYDRATE (CUPRIC SULFATE) POWDER, FOR SOLUTION [FONDEL CHEMICALS LTD.]	4
Cupric Cation	ACTIVE MOIETY	8CBV67279L	CUPRIC SULFATE PENTAHYDRATE (CUPRIC SULFATE) POWDER, FOR SOLUTION [FONDEL CHEMICALS LTD.]	4

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 2 of 2 · 24 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Concept OB	VITAMIN MINERAL SUPPLEMENT	U.S. Pharmaceutical Corporation	37992a25-68bd-4050-b936-596ddedc25a3	2022-11-08	Warnings, Adverse reactions	Exact identifier unii: LRX7AJ16DT
Cuprum Sulphuricum	CUPRUM SULPHURICUM	OHM PHARMA INC.	7753dbf1-4cce-4a5e-a7d2-549574828268	2021-12-30	Warnings	Exact identifier unii: LRX7AJ16DT
Multitrace -4 Pediatric	TRACE ELEMENTS 4	American Regent, Inc.	5ee6a685-3c35-467b-8d4d-79efdd0bfa8e	2019-04-25	Warnings, Adverse reactions	Exact identifier unii: LRX7AJ16DT
Multitrace-5	TRACE ELEMENTS 5	American Regent, Inc.	ef63bbe8-ebf8-436c-b38d-6cb92bc91ac0	2019-04-25	Warnings, Adverse reactions	Exact identifier unii: LRX7AJ16DT

Reported adverse events (FAERS/openFDA)#

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