NDC 55259-0003 Hantai 8030 Ca-d3 Premium

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:
55259-0003
Proprietary Name:
Hantai 8030 Ca-d3 Premium
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Apexel Co., Ltd.
Labeler Code:
55259
Start Marketing Date: [9]
03-18-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
OVAL (C48345)
Size(s):
12 MM

Product Packages

NDC Code 55259-0003-2

Package Description: 1 BOTTLE in 1 PACKAGE / 120 TABLET in 1 BOTTLE

Product Details

What is NDC 55259-0003?

The NDC code 55259-0003 is assigned by the FDA to the product Hantai 8030 Ca-d3 Premium which is product labeled by Apexel Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 55259-0003-2 1 bottle in 1 package / 120 tablet in 1 bottle. 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 Hantai 8030 Ca-d3 Premium?

This product is used as To prevent and cure the osteoporosis, cardiovascular disorders, depression, nerve stability, muscle pain, arthritis, menstrual pain, ostalgia and promote growth and healing.. Take one tablet every time, two times a day with enough water.

Which are Hantai 8030 Ca-d3 Premium UNII Codes?

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

Which are Hantai 8030 Ca-d3 Premium 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:

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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".