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NDC 17238-920 Greenglo

Lissamine Green Strip Ophthalmic - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 17238-920?
  4. Greenglo Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes

Product Information

NDC Product Code:
17238-920
Proprietary Name:
Greenglo
Non-Proprietary Name: [1]
Lissamine Green
Substance Name: [2]
Light Green Sf Yellowish
NDC Directory Status:
Human Prescription Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Strip - A long narrow piece of material.
Administration Route(s): [4]
  • Ophthalmic - Administration to the external eye.
    • Labeler Name: [5]
    Hub Pharmaceuticals, Inc.
    Labeler Code:
    17238
    Product Label ID:
    16a8622b-b349-4b10-b45a-f1f1551b2b06
    Marketing Category: [8]
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date: [9]
    04-01-2012
    Listing Expiration Date: [11]
    12-31-2025
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 17238-920-11

    Package Description: 100 PACKET in 1 BOX / 1.5 mg in 1 PACKET (17238-920-99)

    Product Details

    What is NDC 17238-920?

    The NDC code 17238-920 is assigned by the FDA to the product Greenglo which is a human prescription drug product labeled by Hub Pharmaceuticals, Inc.. The generic name of Greenglo is lissamine green. The product's dosage form is strip and is administered via ophthalmic form. The product is distributed in a single package with assigned NDC code 17238-920-11 100 packet in 1 box / 1.5 mg in 1 packet (17238-920-99). 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 Greenglo?

    For use as a diagnostic agent when superficial corneal or conjunctival tissue change is suspected.

    What are Greenglo Active Ingredients?

    An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    Which are Greenglo UNII Codes?

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

    • LIGHT GREEN SF YELLOWISH (UNII: 3F7BHA64Z0)
    • LIGHT GREEN SF YELLOWISH (UNII: 3F7BHA64Z0) (Active Moiety)

    * Please review the disclaimer below.

    Product Footnotes

    [1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

    [2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    [3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

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

    [8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

    [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".