NDC 50090-0765 Clarinex
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50090 - A-s Medication Solutions
- 50090-0765 - Clarinex
Product Characteristics
Product Packages
NDC Code 50090-0765-0
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE
Product Details
What is NDC 50090-0765?
What are the uses for Clarinex?
Which are Clarinex UNII Codes?
The UNII codes for the active ingredients in this product are:
- DESLORATADINE (UNII: FVF865388R)
- DESLORATADINE (UNII: FVF865388R) (Active Moiety)
Which are Clarinex 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:
- DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- STARCH, CORN (UNII: O8232NY3SJ)
- TALC (UNII: 7SEV7J4R1U)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- WHITE WAX (UNII: 7G1J5DA97F)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- ALUMINUM OXIDE (UNII: LMI26O6933)
What is the NDC to RxNorm Crosswalk for Clarinex?
- RxCUI: 349420 - desloratadine 5 MG Oral Tablet
- RxCUI: 352086 - CLARINEX 5 MG Oral Tablet
- RxCUI: 352086 - desloratadine 5 MG Oral Tablet [Clarinex]
- RxCUI: 352086 - Clarinex 5 MG Oral Tablet
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Patient Education
Desloratadine
Desloratadine is used in adults and children to relieve hay fever and allergy symptoms, including sneezing; runny nose; and red, itchy, tearing eyes. It is also used to relieve symptoms of urticaria (hives; red, itchy raised areas of the skin), including itching and rash. Desloratadine is in a class of medications called antihistamines. It works by blocking histamine, a substance in the body that causes allergic symptoms.
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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".