NDC 50594-769 Fexofenadine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50594 - Big Lots Stores, Inc.
- 50594-769 - Fexofenadine Hydrochloride
Product Characteristics
Product Packages
NDC Code 50594-769-03
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE
Product Details
What is NDC 50594-769?
What are the uses for Fexofenadine Hydrochloride?
Which are Fexofenadine Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- FEXOFENADINE HYDROCHLORIDE (UNII: 2S068B75ZU)
- FEXOFENADINE (UNII: E6582LOH6V) (Active Moiety)
Which are Fexofenadine Hydrochloride 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:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- CROSCARMELLOSE (UNII: 029TFK992N)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- STARCH, PREGELATINIZED CORN (UNII: O8232NY3SJ)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
What is the NDC to RxNorm Crosswalk for Fexofenadine Hydrochloride?
- RxCUI: 997420 - fexofenadine HCl 180 MG 24 HR Oral Tablet
- RxCUI: 997420 - fexofenadine hydrochloride 180 MG Oral Tablet
* Please review the disclaimer below.
Patient Education
Fexofenadine
Fexofenadine is used to relieve the allergy symptoms of seasonal allergic rhinitis (''hay fever''), including runny nose; sneezing; red, itchy, or watery eyes; or itching of the nose, throat, or roof of the mouth in adults and children 2 years of age and older. It is also used to relieve symptoms of urticaria (hives; red, itchy raised areas of the skin), including itching and rash in adults and children 6 months of age and older. Fexofenadine is in a class of medications called antihistamines. It works by blocking the effects of histamine, a substance in the body that causes allergy 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".