NDC 63672-0051 Levocetirizine Dihydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63672 - Synthon Pharmaceuticals, Inc.
- 63672-0051 - Levocetirizine Dihydrochloride
Product Characteristics
Product Packages
NDC Code 63672-0051-0
Package Description: 87000 TABLET, FILM COATED in 1 DRUM
Product Details
What is NDC 63672-0051?
What are the uses for Levocetirizine Dihydrochloride?
Which are Levocetirizine Dihydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- LEVOCETIRIZINE DIHYDROCHLORIDE (UNII: SOD6A38AGA)
- LEVOCETIRIZINE (UNII: 6U5EA9RT2O) (Active Moiety)
Which are Levocetirizine Dihydrochloride 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)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
What is the NDC to RxNorm Crosswalk for Levocetirizine Dihydrochloride?
- RxCUI: 855172 - levocetirizine dihydrochloride 5 MG Oral Tablet
- RxCUI: 855172 - levocetirizine dihydrochloride 5 MG 24 HR 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".