NDC 21695-076 Meloxicam

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:
21695-076
Proprietary Name:
Meloxicam
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rebel Distributors Corp.
Labeler Code:
21695
Start Marketing Date: [9]
12-20-2006
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330)
Shape:
ROUND (C48348)
Size(s):
6 MM
Imprint(s):
APO;MEL;7
Score:
1

Product Packages

NDC Code 21695-076-14

Package Description: 14 TABLET in 1 BOTTLE, PLASTIC

NDC Code 21695-076-15

Package Description: 15 TABLET in 1 BOTTLE, PLASTIC

NDC Code 21695-076-30

Package Description: 30 TABLET in 1 BOTTLE, PLASTIC

NDC Code 21695-076-60

Package Description: 60 TABLET in 1 BOTTLE, PLASTIC

NDC Code 21695-076-90

Package Description: 90 TABLET in 1 BOTTLE, PLASTIC

Product Details

What is NDC 21695-076?

The NDC code 21695-076 is assigned by the FDA to the product Meloxicam which is product labeled by Rebel Distributors Corp.. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 21695-076-14 14 tablet in 1 bottle, plastic , 21695-076-15 15 tablet in 1 bottle, plastic , 21695-076-30 30 tablet in 1 bottle, plastic , 21695-076-60 60 tablet in 1 bottle, plastic , 21695-076-90 90 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 Meloxicam?

Meloxicam is used to treat arthritis. It reduces pain, swelling, and stiffness of the joints. Meloxicam is known as a nonsteroidal anti-inflammatory drug (NSAID). If you are treating a chronic condition such as arthritis, ask your doctor about non-drug treatments and/or using other medications to treat your pain. See also Warning section.

Which are Meloxicam UNII Codes?

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

Which are Meloxicam 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 Meloxicam?

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:

* Please review the disclaimer below.

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".