NDC 68554-5062 Fexofenadine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
OVAL (C48345)
12 MM
J;43
Code Structure Chart
Product Details
What is NDC 68554-5062?
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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- STARCH, CORN (UNII: O8232NY3SJ)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- LIGHT MINERAL OIL (UNII: N6K5787QVP)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- 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
- RxCUI: 997488 - fexofenadine HCl 30 MG Oral Tablet
- RxCUI: 997488 - fexofenadine hydrochloride 30 MG Oral Tablet
- RxCUI: 997501 - fexofenadine HCl 60 MG Oral Tablet
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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".