Nephron FA

Manufacturer
Nephro-Tech, Inc. | LGM Pharma
Effective date
2021-07-08
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
10
Source
full-release
Hydrated at
2026-05-31 20:37:23

Label at a glance#

ProductNephron FA
Active ingredientIRON, ASCORBIC ACID, NIACINAMIDE, PYRIDOXINE HYDROCHLORIDE, PANTOTHENIC ACID, RIBOFLAVIN, THIAMINE, FOLIC ACID, Biotin, COBALAMIN
Label structure4 sections

Label contents#

Full prescribing information#

Description

DESCRIPTION SECTION

Nephron FA is a prescription folic acid supplement with additional nutrients for kidney dialysis patients.  Nephron FA is an elongated, white, film coated tablet imprinted with NT and scored on one side, plain on the other.

Precaution

PRECAUTIONS SECTION

Folic Acid may obscure pernicious anemia or produce remission while neurologic progress may continue.

Suggested Dosage

DOSAGE & ADMINISTRATION SECTION

One tablet daily taken away from meals, or as directed by the physician.

Package Label/Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Nephron FA label

59528-4456-1

Rx Only

Nephron FA

Vitamin/Mineral Supplement

100 tablets

Nephron FA labelNephron FA label

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
ASCORBIC ACID Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813
PYRIDOXINE Pharmacologic Class Indexing1Indexing - Pharmacologic Class20170310

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
cf050ccd-1144-f76a-e00d-e5698d8597d4Product name620250625
59361619-24d9-b610-eca6-5a7f25ed5e03Product name520240909
910c1bd7-67d1-44c7-ad4f-9445f827edccProduct name120230808
91c62db0-0295-c81c-d10a-0856c259edd6Product name220200428
d32bc2b8-0bb7-2216-87aa-24639646e202Product name320190619
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122
5e18e798-5614-cf5c-0185-38b1cb77a093Product name220160822

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59528-4456-1Nephron FA100 in 1 BOTTLE, PLASTICTABLET, COATED10010

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59528-4456NEPHRON FA (MINERAL/VITAMIN SUPPLEMENT) TABLET, COATED [NEPHRO-TECH, INC.]10Legacy NDC, 1 package rows20210715_a709f56a-08d0-4fe5-a9ed-e237a745be97.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
59528-4456-1EA - Each59528-44568abf13da-9691-4098-9859-4c3b6e2af3d012014-07-02

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ASCORBIC ACIDACTIVE INGREDIENTPQ6CK8PD0R1
BiotinACTIVE INGREDIENT6SO6U10H041
COBALAMINACTIVE INGREDIENT8406EY2OQA1
FOLIC ACIDACTIVE INGREDIENT935E97BOY81
IRONACTIVE INGREDIENTE1UOL152H71
NIACINAMIDEACTIVE INGREDIENT25X51I8RD41
PANTOTHENIC ACIDACTIVE INGREDIENT19F5HK27371
PYRIDOXINE HYDROCHLORIDEACTIVE INGREDIENT68Y4CF58BV1
RIBOFLAVINACTIVE INGREDIENTTLM2976OFR1
THIAMINEACTIVE INGREDIENTX66NSO3N351
ASCORBIC ACIDACTIVE MOIETYPQ6CK8PD0R1
BIOTINACTIVE MOIETY6SO6U10H041
COBALAMINACTIVE MOIETY8406EY2OQA1
FERROUS CATIONACTIVE MOIETYGW89581OWR1
FOLIC ACIDACTIVE MOIETY935E97BOY81
NIACINAMIDEACTIVE MOIETY25X51I8RD41
PANTOTHENIC ACIDACTIVE MOIETY19F5HK27371
PYRIDOXINEACTIVE MOIETYKV2JZ1BI6Z1
RIBOFLAVINACTIVE MOIETYTLM2976OFR1
THIAMINE IONACTIVE MOIETY4ABT0J945J1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59528-445659528-4456-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Source Document#

Source XML · Source PDF

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 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
43a37439-b71f-4894-b7a1-f8d0af2c1212a709f56a-08d0-4fe5-a9ed-e237a745be972021-07-08Exact identifier
spl id: 43a37439-b71f-4894-b7a1-f8d0af2c1212
spl set id: a709f56a-08d0-4fe5-a9ed-e237a745be97

Reported adverse events (FAERS/openFDA)#

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