NDC 69313-634 Lidoflex

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:
69313-634
Proprietary Name:
Lidoflex
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Naimco, Inc. Dba Richmar, Inc.
Labeler Code:
69313
Start Marketing Date: [9]
09-01-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 69313-634-01

Package Description: 22.7 mg in 1 POUCH

NDC Code 69313-634-05

Package Description: 22.7 mg in 1 BAG

NDC Code 69313-634-20

Package Description: 22.7 mg in 1 PACKAGE

Product Details

What is NDC 69313-634?

The NDC code 69313-634 is assigned by the FDA to the product Lidoflex which is product labeled by Naimco, Inc. Dba Richmar, Inc.. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 69313-634-01 22.7 mg in 1 pouch , 69313-634-05 22.7 mg in 1 bag , 69313-634-20 22.7 mg in 1 package . 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 Lidoflex?

Use For the temporary relief of pain.

Which are Lidoflex UNII Codes?

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

Which are Lidoflex 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:

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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".