NDC 53144-1001 Mesima

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:
53144-1001
Proprietary Name:
Mesima
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
53144
Start Marketing Date: [9]
12-29-2012
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
BROWN (C48332 - LIGHT BROWN)
Shape:
OVAL (C48345)
Size(s):
15 MM
Imprint(s):
3;HP;X
Score:
1

Code Structure Chart

Product Details

What is NDC 53144-1001?

The NDC code 53144-1001 is assigned by the FDA to the product Mesima which is product labeled by Yein Trading & Global Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 53144-1001-1 2 capsule in 1 package . 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 Mesima?

- effective in uterine discharge and bleeding, dysmenorrheal, intestinal bleeding, and activation of GI system, 550-1100mg twice a day before meals- effective in improving the immune functions of cancer patients after surgical resection of stomach, colon, or liver, 1100mg three times a day before meals

Which are Mesima UNII Codes?

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

  • PHELLINUS LINTEUS MYCELIUM (UNII: 40K19XJV3C)
  • PHELLINUS LINTEUS MYCELIUM (UNII: 40K19XJV3C) (Active Moiety)

Which are Mesima 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".