NDC 15014-211 Hidex 6-day
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 15014 - Gentex Pharma, Llc
- 15014-211 - Hidex 6-day
Product Characteristics
Product Packages
NDC Code 15014-211-21
Package Description: 1 BLISTER PACK in 1 CARTON / 21 TABLET in 1 BLISTER PACK
Product Details
What is NDC 15014-211?
What are the uses for Hidex 6-day?
Which are Hidex 6-day UNII Codes?
The UNII codes for the active ingredients in this product are:
- DEXAMETHASONE (UNII: 7S5I7G3JQL)
- DEXAMETHASONE (UNII: 7S5I7G3JQL) (Active Moiety)
Which are Hidex 6-day 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:
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
What is the NDC to RxNorm Crosswalk for Hidex 6-day?
- RxCUI: 197580 - dexAMETHasone 1.5 MG Oral Tablet
- RxCUI: 197580 - dexamethasone 1.5 MG Oral Tablet
- RxCUI: 2118829 - {21 (dexamethasone 1.5 MG Oral Tablet) } Pack [HiDex 6-Day Taper]
- RxCUI: 2118829 - HiDex 1.5 MG Tablet 6-day 21 Count Taper Pack
- RxCUI: 846192 - {21 (dexamethasone 1.5 MG Oral Tablet) } Pack
* Please review the disclaimer below.
Patient Education
Dexamethasone
Dexamethasone, a corticosteroid, is similar to a natural hormone produced by your adrenal glands. It often is used to replace this chemical when your body does not make enough of it. It relieves inflammation (swelling, heat, redness, and pain) and is used to treat certain forms of arthritis; skin, blood, kidney, eye, thyroid, and intestinal disorders (e.g., colitis); severe allergies; and asthma. Dexamethasone is also used to treat certain types of cancer. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
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* Please review the disclaimer below.
[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".