NDC 53002-6060 Meclizine Hcl 12.5 Mg
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53002 - Rpk Pharmaceuticals, Inc.
- 53002-6060 - Meclizine Hcl 12.5 Mg
Product Characteristics
Product Packages
NDC Code 53002-6060-1
Package Description: 10 TABLET in 1 BOTTLE
NDC Code 53002-6060-2
Package Description: 20 TABLET in 1 BOTTLE
NDC Code 53002-6060-3
Package Description: 30 TABLET in 1 BOTTLE
Product Details
What is NDC 53002-6060?
What are the uses for Meclizine Hcl 12.5 Mg?
Which are Meclizine Hcl 12.5 Mg 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 Hcl 12.5 Mg 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)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)
What is the NDC to RxNorm Crosswalk for Meclizine Hcl 12.5 Mg?
- RxCUI: 995624 - meclizine HCl 12.5 MG Oral Tablet
- RxCUI: 995624 - meclizine hydrochloride 12.5 MG Oral Tablet
* Please review the disclaimer below.
Patient Education
Meclizine
Meclizine is used to prevent and treat nausea, vomiting, and dizziness caused by motion sickness. It is most effective if taken before symptoms appear.
[Learn More]
* 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".