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  4. NDC Product Code: 71384-512 Dex-moxi

NDC 71384-512 Dex-moxi

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71384-512?
  4. 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:
71384-512
Proprietary Name:
Dex-moxi
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Imprimis Njof, Llc
Labeler Code:
71384
Product Label ID:
62ff1da3-7998-676a-e053-2991aa0a4a9f
Start Marketing Date: [9]
01-05-2018
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 71384-512?

The NDC code 71384-512 is assigned by the FDA to the product Dex-moxi which is product labeled by Imprimis Njof, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71384-512-01 20 vial, single-use in 1 box / 1 ml in 1 vial, single-use. 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 Dex-moxi UNII Codes?

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

  • DEXAMETHASONE SODIUM PHOSPHATE (UNII: AI9376Y64P)
  • DEXAMETHASONE (UNII: 7S5I7G3JQL) (Active Moiety)
  • MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE (UNII: B8956S8609)
  • MOXIFLOXACIN (UNII: U188XYD42P) (Active Moiety)

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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".