Nephron FA

NEPHRON FA- iron, ascorbic acid, niacinamide, pyridoxine hydrochloride, pantothenic acid, riboflavin, thiamine, folic acid, biotin and cobalamin tablet, coated
Nephro-Tech, Inc.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Description

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

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

Suggested Dosage

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

Package Label/Principal Display Panel

Nephron FA label

59528-4456-1

Rx Only

Nephron FA

Vitamin/Mineral Supplement

100 tablets

Nephron FA label
(click image for full-size original)
NEPHRON FA
mineral/vitamin supplement tablet, coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:59528-4456
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
IRON (FERROUS CATION) FERROUS CATION 66 mg
ASCORBIC ACID (ASCORBIC ACID) ASCORBIC ACID 40 mg
NIACINAMIDE (NIACINAMIDE) NIACINAMIDE 20 mg
PYRIDOXINE HYDROCHLORIDE (PYRIDOXINE) PYRIDOXINE HYDROCHLORIDE 10 mg
PANTOTHENIC ACID (PANTOTHENIC ACID) PANTOTHENIC ACID 10 mg
RIBOFLAVIN (RIBOFLAVIN) RIBOFLAVIN 1.7 mg
THIAMINE (THIAMINE ION) THIAMINE 1.5 mg
FOLIC ACID (FOLIC ACID) FOLIC ACID 1 mg
Biotin (BIOTIN) Biotin .3 mg
COBALAMIN (COBALAMIN) COBALAMIN .006 mg
Product Characteristics
Color white Score 2 pieces
Shape capsule Size 19mm
Flavor Imprint Code NT
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:59528-4456-1 100 TABLET, COATED in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 11/01/1992
Labeler — Nephro-Tech, Inc. (878520485)
Registrant — Nephro-Tech, Inc. (878520485)
Establishment
Name Address ID/FEI Operations
LGM Pharma 117549200 manufacture (59528-4456)

Revised: 07/2021 Nephro-Tech, Inc.

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