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  4. NDC Product Code: 64725-5896 Nicotine

NDC 64725-5896 Nicotine

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 64725-5896?
  4. Nicotine Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
64725-5896
Proprietary Name:
Nicotine
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Tya Pharmaceuticals
Labeler Code:
64725
Product Label ID:
9265d2b3-1f87-45ea-ba0a-5192175b4309
Start Marketing Date: [9]
10-20-1997
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 64725-5896?

The NDC code 64725-5896 is assigned by the FDA to the product Nicotine which is product labeled by Tya Pharmaceuticals. The product's dosage form is . The product is distributed in a single package with assigned NDC code 64725-5896-1 14 h in 1 box . 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 Nicotine?

If you are under 18 years of age, ask a doctor before useBefore using this product, read the enclosed self-help guide for complete directions and other informationStop smoking completely when you begin using the patchIf you smoke more than 10 cigarettes per day, use the following schedule:Weeks 1 thru 4Weeks 5 and 6Weeks 7 and 8STEP 1STEP 2STEP 3use one 21 mg patch/dayuse one 14 mg patch/dayuse one 7 mg patch/dayIf you smoke 10 or start with for 6 weeks, then for 2 weeks and then stop less cigarettes per day,Step 2Step 3Apply one new patch every 24 hours on skin that is dry, clean, and hairlessRemove backing from patch and immediately press onto skin. Hold for 10 seconds.Wash hands after applying or removing patch. Save pouch to use for patch disposal. Dispose of used patch by folding sticky ends together and putting in pouch.The used patch should be removed and a new one applied to a different skin site at the same time each dayIf you have vivid dreams, you may remove the patch at bedtime and apply a new one in the morningDo not wear more than one patch at a timeDo not cut patch in half or into smaller piecesDo not leave patch on for more than 24 hours because it may irritate your skin and loses strength after 24 hoursStop using the patch at the end of 8 weeks. If you still feel the need to use the patch talk to your doctor.

Which are Nicotine UNII Codes?

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

Which are Nicotine 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 Nicotine?

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".