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  4. NDC Product Code: 42546-180 Bal-care Dha

NDC 42546-180 Bal-care Dha

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 42546-180?
  5. Active Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
42546-180
Proprietary Name:
Bal-care Dha
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Prugen, Inc.
Labeler Code:
42546
Product Label ID:
b2f0ca0d-76e9-45f0-bf60-e9781c227676
Start Marketing Date: [9]
05-01-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
PINK (C48328)
BROWN (C48332)
Shape:
OVAL (C48345)
Size(s):
19 MM
24 MM
Imprint(s):
102
NONE
Score:
1

Code Structure Chart

Product Details

What is NDC 42546-180?

The NDC code 42546-180 is assigned by the FDA to the product Bal-care Dha which is product labeled by Prugen, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 42546-180-30 6 blister pack in 1 carton / 1 kit in 1 blister pack. 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.

Which are Bal-care Dha UNII Codes?

The UNII codes for the active 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".