NDC 0440-1736 Meclizine Hydrochloride

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
0440-1736
Proprietary Name:
Meclizine Hydrochloride
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Liberty Pharmaceuticals, Inc.
Labeler Code:
0440
Start Marketing Date: [9]
06-03-1981
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330)
Shape:
OVAL (C48345)
Size(s):
6 MM
Imprint(s):
PAR;035
Score:
1

Product Packages

NDC Code 0440-1736-08

Package Description: 8 TABLET in 1 BOTTLE, PLASTIC

Product Details

What is NDC 0440-1736?

The NDC code 0440-1736 is assigned by the FDA to the product Meclizine Hydrochloride which is product labeled by Liberty Pharmaceuticals, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 0440-1736-08 8 tablet in 1 bottle, plastic . 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 Meclizine Hydrochloride?

INDICATIONSBased on a review of this drug by the National Academy of Sciences – National Research Council and/or other information, FDA has classified the indications as follows:Effective: Management of nausea and vomiting, and dizziness associated with motion sickness.Possibly Effective: Management of vertigo associated with diseases affecting the vestibular system.Final classification of the less than effective indications required further investigation.

Which are Meclizine Hydrochloride UNII Codes?

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

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:

What is the NDC to RxNorm Crosswalk for Meclizine Hydrochloride?

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:

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Product Footnotes

[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".