NDC 0517-6502-01 - Selenious 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: 0517-6502
Requested NDC: 0517-6502-01
Package NDCs from labels: 0517-6502-01, 0517-6502-10
Manufacturer: American Regent, Inc.
Effective date: 2021-08-01
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Selenious Acid - American Regent, Inc.	American Regent, Inc.	2021-08-01	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0517-6502-01	Selenious Acid	2 mL in 1 VIAL, SINGLE-DOSE	INJECTION, SOLUTION	2		13
0517-6502-10	Selenious Acid	10 in 1 BOX	INJECTION, SOLUTION	10		13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0517-6502	SELENIOUS ACID INJECTION, SOLUTION [AMERICAN REGENT, INC.]	13	Current NDC, Legacy NDC, 2 package rows	20240112_49324999-50e3-43ed-a8dd-156d6dbedd9f.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0517-6502-01	ML - Milliliter	0517-6502	1d152a90-47fb-4755-a06d-d8aab119a24c	1	2022-02-07
0517-6502-10	ML - Milliliter	0517-6502	ed79954d-3181-45f2-bfc5-537d344d655a	1	2022-02-07

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 27 of 27 · 525 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Industrotox	GLYCYRRHIZA GLABRA, PLANTAGO MAJOR, STILLINGIA SYLVATICA, TRIFOLIUM PRATENSE, ARNICA MONTANA, ASCLEPIAS TUBEROSA, BERBERIS VULGARIS, CALENDULA OFFICINALIS, CHAMOMILLA, CHELIDONIUM MAJUS, ECHINACEA (ANGUSTIFOLIA), EUCALYPTUS GLOBULUS, LAPPA MAJOR, NASTURTIUM AQUATICUM, PHYTOLACCA DECANDRA, RHAMNUS FRANGULA, RHAMNUS PURSHIANA, TARAXACUM OFFICINALE, TRIGONELLA FOENUM-GRAECUM, URTICA DIOICA, XANTHOXYLUM FRAXINEUM, SYMPHYTUM OFFICINALE, HEPAR SUIS, LUNG (SUIS), LYMPH NODE (SUIS)	BioActive Nutritional, Inc.	0722085a-1478-4667-b0c6-3315cff25b08	2017-06-16	Warnings	Exact identifier unii: 411VRN1TV4
Enuresis	EQUISETUM HYEMALE, SOLIDAGO VIRGAUREA, UVA-URSI, ARGENTUM METALLICUM, CAUSTICUM, KREOSOTUM, NITRICUM ACIDUM, SEPIA, THUJA OCCIDENTALIS	BioActive Nutritional, Inc.	22105dde-b570-4af6-a7b8-e942f649e934	2017-06-14	Warnings	Exact identifier unii: 411VRN1TV4
Eye Wash	WATER	CVS Pharmacy	049cee29-7ec2-4d5b-8308-f522acde43a7	2017-03-29	Warnings	Exact identifier unii: 059QF0KO0R
Enuresis HP	ARGENTUM NITRICUM, BELLADONNA, CAUSTICUM, EQUISETUM HYEMALE, KREOSOTUM, NITRICUM ACIDUM, PULSATILLA (VULGARIS), THUJA OCCIDENTALIS	BioActive Nutritional, Inc.	a6fff9be-e78d-4539-b741-6a8080a164a0	2016-09-07	Warnings	Exact identifier unii: 411VRN1TV4
Sterile Water	WATER	Baxter Healthcare Company	210dc9ab-d6ca-4552-ac19-1be17792d290	2016-05-31	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R

Reported adverse events (FAERS/openFDA)#

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