NDC 0363-1407 Wal-dram 2 Quick-dissolving

Meclizine Hydrochloride Tablet, Orally Disintegrating Oral - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
0363-1407
Proprietary Name:
Wal-dram 2 Quick-dissolving
Non-Proprietary Name: [1]
Meclizine Hydrochloride
Substance Name: [2]
Meclizine Hydrochloride
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Tablet, Orally Disintegrating - A solid dosage form containing medicinal substances which disintegrates rapidly, usually within a matter of seconds, when placed upon the tongue.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
  • Labeler Name: [5]
    Walgreen Co.
    Labeler Code:
    0363
    FDA Application Number: [6]
    M009
    Marketing Category: [8]
    OTC MONOGRAPH DRUG -
    Start Marketing Date: [9]
    03-01-2016
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Characteristics

    Color(s):
    YELLOW (C48330)
    Shape:
    ROUND (C48348)
    Size(s):
    13 MM
    Imprint(s):
    SJ
    Score:
    1

    Product Packages

    NDC Code 0363-1407-01

    Package Description: 2 BLISTER PACK in 1 CARTON / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

    NDC Code 0363-1407-02

    Package Description: 3 BLISTER PACK in 1 CARTON / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

    Product Details

    What is NDC 0363-1407?

    The NDC code 0363-1407 is assigned by the FDA to the product Wal-dram 2 Quick-dissolving which is a human over the counter drug product labeled by Walgreen Co.. The generic name of Wal-dram 2 Quick-dissolving is meclizine hydrochloride. The product's dosage form is tablet, orally disintegrating and is administered via oral form. The product is distributed in 2 packages with assigned NDC codes 0363-1407-01 2 blister pack in 1 carton / 6 tablet, orally disintegrating in 1 blister pack, 0363-1407-02 3 blister pack in 1 carton / 6 tablet, orally disintegrating in 1 blister pack. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

    What are the uses for Wal-dram 2 Quick-dissolving?

    Uses■ For the prevention and treatment of the nausea, vomiting, or dizziness associated with motion sickness.

    What are Wal-dram 2 Quick-dissolving Active Ingredients?

    An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
    • MECLIZINE HYDROCHLORIDE 25 mg/1 - A histamine H1 antagonist used in the treatment of motion sickness, vertigo, and nausea during pregnancy and radiation sickness.

    Which are Wal-dram 2 Quick-dissolving UNII Codes?

    The UNII codes for the active ingredients in this product are:

    Which are Wal-dram 2 Quick-dissolving 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:

    What is the NDC to RxNorm Crosswalk for Wal-dram 2 Quick-dissolving?

    RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
    • RxCUI: 1663815 - meclizine HCl 25 MG Disintegrating Oral Tablet
    • RxCUI: 1663815 - meclizine hydrochloride 25 MG Disintegrating Oral Tablet
    • RxCUI: 1800794 - Wal-Dram 2 25 MG Disintegrating Oral Tablet
    • RxCUI: 1800794 - meclizine hydrochloride 25 MG Disintegrating Oral Tablet [Wal-Dram 2]

    Which are the Pharmacologic Classes for Wal-dram 2 Quick-dissolving?

    A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

    * 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.

    Product Footnotes

    [1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

    [2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    [3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

    [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".