NDC 68071-4002 Fluconazole
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68071 - Nucare Pharmaceuticals,inc.
- 68071-4002 - Fluconazole
Product Characteristics
Product Packages
NDC Code 68071-4002-1
Package Description: 1 TABLET in 1 BLISTER PACK
Product Details
What is NDC 68071-4002?
What are the uses for Fluconazole?
Which are Fluconazole UNII Codes?
The UNII codes for the active ingredients in this product are:
- FLUCONAZOLE (UNII: 8VZV102JFY)
- FLUCONAZOLE (UNII: 8VZV102JFY) (Active Moiety)
Which are Fluconazole 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:
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: L11K75P92J)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POVIDONES (UNII: FZ989GH94E)
What is the NDC to RxNorm Crosswalk for Fluconazole?
- RxCUI: 197699 - fluconazole 150 MG Oral Tablet
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Patient Education
Fluconazole
Fluconazole is used to treat fungal infections, including yeast infections of the vagina, mouth, throat, esophagus (tube leading from the mouth to the stomach), abdomen (area between the chest and waist), lungs, blood, and other organs. Fluconazole is also used to treat meningitis (infection of the membranes covering the brain and spine) caused by fungus. Fluconazole is also used to prevent yeast infections in patients who are likely to become infected because they are being treated with chemotherapy or radiation therapy before a bone marrow transplant (replacement of unhealthy spongy tissue inside the bones with healthy tissue). Fluconazole is in a class of antifungals called triazoles. It works by slowing the growth of fungi that cause infection.
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[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".