NDC 53808-0380 Meclizine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53808 - State Of Florida Doh Central Pharmacy
- 53808-0380 - Meclizine Hydrochloride
Product Characteristics
Product Packages
NDC Code 53808-0380-1
Package Description: 30 TABLET in 1 BLISTER PACK
Product Details
What is NDC 53808-0380?
What are the uses for Meclizine Hydrochloride?
Which are Meclizine Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- MECLIZINE HYDROCHLORIDE (UNII: HDP7W44CIO)
- MECLIZINE (UNII: 3L5TQ84570) (Active Moiety)
Which are Meclizine 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)
- LACTOSE (UNII: J2B2A4N98G)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- STARCH, CORN (UNII: O8232NY3SJ)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
What is the NDC to RxNorm Crosswalk for Meclizine Hydrochloride?
- RxCUI: 995666 - meclizine HCl 25 MG Oral Tablet
- RxCUI: 995666 - meclizine hydrochloride 25 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".