NDC 54868-5419 Allegra--d 24 Hour
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
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Product Details
What is NDC 54868-5419?
What are the uses for Allegra--d 24 Hour?
Which are Allegra--d 24 Hour UNII Codes?
The UNII codes for the active ingredients in this product are:
- FEXOFENADINE HYDROCHLORIDE (UNII: 2S068B75ZU)
- FEXOFENADINE (UNII: E6582LOH6V) (Active Moiety)
- PSEUDOEPHEDRINE HYDROCHLORIDE (UNII: 6V9V2RYJ8N)
- PSEUDOEPHEDRINE (UNII: 7CUC9DDI9F) (Active Moiety)
Which are Allegra--d 24 Hour 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:
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CELLULOSE ACETATE (UNII: 3J2P07GVB6)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- POVIDONE (UNII: FZ989GH94E)
- TALC (UNII: 7SEV7J4R1U)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- COPOVIDONE (UNII: D9C330MD8B)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- ACETONE (UNII: 1364PS73AF)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- METHYL ALCOHOL (UNII: Y4S76JWI15)
- METHYLENE CHLORIDE (UNII: 588X2YUY0A)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Allegra--d 24 Hour?
- RxCUI: 997415 - fexofenadine HCl 180 MG / pseudoephedrine HCl 240 MG 24HR Extended Release Oral Tablet
- RxCUI: 997415 - 24 HR fexofenadine hydrochloride 180 MG / pseudoephedrine hydrochloride 240 MG Extended Release Oral Tablet
- RxCUI: 997415 - fexofenadine hydrochloride 180 MG / pseudoephedrine hydrochloride 240 MG 24 HR Extended Release Oral Tablet
- RxCUI: 997515 - Allegra-D 180 MG / 240 MG 24HR Extended Release Oral Tablet
- RxCUI: 997515 - 24 HR fexofenadine hydrochloride 180 MG / pseudoephedrine hydrochloride 240 MG Extended Release Oral Tablet [Allegra-D]
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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".