NDC 68275-320 Colocynthis Homaccord

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:
68275-320
Proprietary Name:
Colocynthis Homaccord
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Jenahexal Pharma Gmbh
Labeler Code:
68275
Start Marketing Date: [9]
09-09-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 68275-320-10

Package Description: 1.1 mL in 1 AMPULE

Product Details

What is NDC 68275-320?

The NDC code 68275-320 is assigned by the FDA to the product Colocynthis Homaccord which is product labeled by Jenahexal Pharma Gmbh. The product's dosage form is . The product is distributed in a single package with assigned NDC code 68275-320-10 1.1 ml in 1 ampule . 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 Colocynthis Homaccord?

Indications and Usage:     •        Colocynthis-Homaccord® Injection Solution is indicated for neuralgia of various origins and locations, especially sciatic neuralgia, intercostal neuralgia and intervertebral disc disorders. 1.     Indications and Usage     1.1    Colocynthis-Homaccord® Injection Solution is classifed as a homeopathic combination drug.     1.2    Botanical ingredients: Colocynthis (bitter cucumber) Gnaphalium polycephalum (common everlasting)     1.3    Colocynthis-Homaccord® Injection Solution is indicated for neuralgia of various origins and locations, especially sciatic neuralgia, intercostal neuralgia and intervertebral disc disorders.

Which are Colocynthis Homaccord UNII Codes?

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

  • GNAPHALIUM (UNII: BGI20Z6M57)
  • GNAPHALIUM (UNII: BGI20Z6M57) (Active Moiety)
  • CITRULLUS COLOCYNTHIS FRUIT WITHOUT SEED (UNII: 23H32AOH17)
  • CITRULLUS COLOCYNTHIS FRUIT WITHOUT SEED (UNII: 23H32AOH17) (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".