NDC 43742-1482 Co-infxn
Anaplasma Phagocytophilum,Babesia Microti,Bartonella Henselae,Borrelia Burgdorferi - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43742 - Deseret Biologicals, Inc.
- 43742-1482 - Co-infxn
Product Packages
NDC Code 43742-1482-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 43742-1482?
What are the uses for Co-infxn?
What are Co-infxn Active Ingredients?
- ANAPLASMA PHAGOCYTOPHILUM 15 [hp_X]/mL - A species of gram-negative bacteria in the genus ANAPLASMA, family ANAPLASMATACEAE, formerly called Ehrlichia phagocytophila or Ehrlichia equi. This organism is tick-borne (IXODES) and causes disease in horses and sheep. In humans, it causes human granulocytic EHRLICHIOSIS.
- BABESIA MICROTI 15 [hp_X]/mL - A species of protozoa infecting humans via the intermediate tick vector IXODES scapularis. The other hosts are the mouse PEROMYSCUS leucopus and meadow vole MICROTUS pennsylvanicus, which are fed on by the tick. Other primates can be experimentally infected with Babesia microti.
- BARTONELLA HENSELAE 15 [hp_X]/mL - A species of gram-negative bacteria that is the etiologic agent of bacillary angiomatosis (ANGIOMATOSIS, BACILLARY). This organism can also be a cause of CAT-SCRATCH DISEASE in immunocompetent patients.
- BORRELIA BURGDORFERI 15 [hp_X]/mL - A specific species of bacteria, part of the BORRELIA BURGDORFERI GROUP, whose common name is Lyme disease spirochete.
- EHRLICHIA CANIS 15 [hp_X]/mL - Species of gram-negative bacteria in the family ANAPLASMATACEAE, causing EHRLICHIOSIS in DOGS. The most common vector is the brown dog tick. It can also cause disease in humans.
- HEPATITIS B VIRUS 15 [hp_C]/mL - The type species of the genus ORTHOHEPADNAVIRUS which causes human HEPATITIS B and is also apparently a causal agent in human HEPATOCELLULAR CARCINOMA. The Dane particle is an intact hepatitis virion, named after its discoverer. Non-infectious spherical and tubular particles are also seen in the serum.
- JAPANESE ENCEPHALITIS VIRUS 15 [hp_X]/mL - A species of FLAVIVIRUS, one of the Japanese encephalitis virus group (ENCEPHALITIS VIRUSES, JAPANESE), which is the etiological agent of Japanese encephalitis found in Asia, southeast Asia, and the Indian subcontinent.
- MYCOPLASMA PNEUMONIAE 15 [hp_X]/mL - Short filamentous organism of the genus Mycoplasma, which binds firmly to the cells of the respiratory epithelium. It is one of the etiologic agents of non-viral primary atypical pneumonia in man.
- NEISSERIA MENINGITIDIS 21 [hp_X]/mL - A species of gram-negative, aerobic BACTERIA. It is a commensal and pathogen only of humans, and can be carried asymptomatically in the NASOPHARYNX. When found in cerebrospinal fluid it is the causative agent of cerebrospinal meningitis (MENINGITIS, MENINGOCOCCAL). It is also found in venereal discharges and blood. There are at least 13 serogroups based on antigenic differences in the capsular polysaccharides; the ones causing most meningitis infections being A, B, C, Y, and W-135. Each serogroup can be further classified by serotype, serosubtype, and immunotype.
Which are Co-infxn UNII Codes?
The UNII codes for the active ingredients in this product are:
- ANAPLASMA PHAGOCYTOPHILUM (UNII: BHE5668847)
- ANAPLASMA PHAGOCYTOPHILUM (UNII: BHE5668847) (Active Moiety)
- BABESIA MICROTI (UNII: 1948X6KEG3)
- BABESIA MICROTI (UNII: 1948X6KEG3) (Active Moiety)
- BARTONELLA HENSELAE (UNII: 84PG7W9845)
- BARTONELLA HENSELAE (UNII: 84PG7W9845) (Active Moiety)
- BORRELIA BURGDORFERI (UNII: 0J8NV9V5Q8)
- BORRELIA BURGDORFERI (UNII: 0J8NV9V5Q8) (Active Moiety)
- EHRLICHIA CANIS (UNII: 970Y8T1JZY)
- EHRLICHIA CANIS (UNII: 970Y8T1JZY) (Active Moiety)
- JAPANESE ENCEPHALITIS VIRUS (UNII: P07E7XWU9D)
- JAPANESE ENCEPHALITIS VIRUS (UNII: P07E7XWU9D) (Active Moiety)
- MYCOPLASMA PNEUMONIAE (UNII: JQE470FAD0)
- MYCOPLASMA PNEUMONIAE (UNII: JQE470FAD0) (Active Moiety)
- NEISSERIA MENINGITIDIS (UNII: V3TP2MD7F3)
- NEISSERIA MENINGITIDIS (UNII: V3TP2MD7F3) (Active Moiety)
- HEPATITIS B VIRUS (UNII: 77H9EM77P7)
- HEPATITIS B VIRUS (UNII: 77H9EM77P7) (Active Moiety)
Which are Co-infxn 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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
* Please review the disclaimer below.
[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.
[10] What is the End Marketing Date? - This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
[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".