NDC 58607-185 Myhephron Dialysis And Stress Supplement

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
58607-185
Proprietary Name:
Myhephron Dialysis And Stress Supplement
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Martin Ekwealor Pharmaceu
Labeler Code:
58607
Start Marketing Date: [9]
08-01-2016
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
BLACK (C48323)
Shape:
CAPSULE (C48336)
Size(s):
18 MM
Imprint(s):
MYNEPHRON;ME185
Score:
1

Product Packages

NDC Code 58607-185-10

Package Description: 100 CAPSULE in 1 BOX

Product Details

What is NDC 58607-185?

The NDC code 58607-185 is assigned by the FDA to the product Myhephron Dialysis And Stress Supplement which is product labeled by Martin Ekwealor Pharmaceu. The product's dosage form is . The product is distributed in a single package with assigned NDC code 58607-185-10 100 capsule in 1 box . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Myhephron Dialysis And Stress Supplement?

Mynephron capsule is indicated in the wasting syndrome of chronic renal failure, uremia and impaired metabolic functions of the kidney, and to maintain levels when the dietary intake of vitamins is inadequate or excretion (loss) is excessive. Mynephron is also highly effective as a stress vitamin.

Which are Myhephron Dialysis And Stress Supplement UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Myhephron Dialysis And Stress Supplement Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".