NDC 50682-527 Lidopatch Pain Relief

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:
50682-527
Proprietary Name:
Lidopatch Pain Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
3t Federal Solutions Llc
Labeler Code:
50682
Start Marketing Date: [9]
02-01-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 50682-527-03

Package Description: 3 POUCH in 1 CARTON / 1 PATCH in 1 POUCH

NDC Code 50682-527-07

Package Description: 7 POUCH in 1 CARTON / 1 PATCH in 1 POUCH

NDC Code 50682-527-30

Package Description: 30 POUCH in 1 CARTON / 1 PATCH in 1 POUCH

Product Details

What is NDC 50682-527?

The NDC code 50682-527 is assigned by the FDA to the product Lidopatch Pain Relief which is product labeled by 3t Federal Solutions Llc. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 50682-527-03 3 pouch in 1 carton / 1 patch in 1 pouch, 50682-527-07 7 pouch in 1 carton / 1 patch in 1 pouch, 50682-527-30 30 pouch in 1 carton / 1 patch in 1 pouch. 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 Lidopatch Pain Relief?

❏adults: apply patch to affected area for a maximum of 12 hours. Do not use more than 1 patch every 24 hours.❏children: consult your physician❏remove protective film, gently apply to affected area.

Which are Lidopatch Pain Relief UNII Codes?

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

Which are Lidopatch Pain Relief 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 Lidopatch Pain Relief?

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".