NDC 42195-490 Taperdex 12-day
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
DEX;1;5
Code Structure Chart
Product Details
What is NDC 42195-490?
What are the uses for Taperdex 12-day?
Which are Taperdex 12-day UNII Codes?
The UNII codes for the active ingredients in this product are:
- DEXAMETHASONE (UNII: 7S5I7G3JQL)
- DEXAMETHASONE (UNII: 7S5I7G3JQL) (Active Moiety)
Which are Taperdex 12-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 Taperdex 12-day?
- RxCUI: 1943550 - {49 (dexamethasone 1.5 MG Oral Tablet) } Pack
- RxCUI: 1943550 - dexAMETHasone 1.5 MG Tablet 12 Day 49 Count Pack
- RxCUI: 1943550 - dexamethasone 1.5 MG Tablet 12 Day 49 Count Pack
- RxCUI: 197580 - dexAMETHasone 1.5 MG Oral Tablet
- RxCUI: 197580 - dexamethasone 1.5 MG Oral Tablet
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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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[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".