Kaydia Patch
NDC Package 75140-002-01
Package Information
Kaydia Patch is 1.Remove backing film 2.Apply patch on dry and clean skin 3.Remove and discard patch after 8-10 hours. Marketed by Strong Current Enterprises Limited, this product is identified by NDC 75140-002.
Identification & Billing
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 75140 - Strong Current Enterprises Limited
- 75140-002 - Kaydia Patch
- 75140-002-01 - 166 g in 1 BOX
- 75140-002 - Kaydia Patch
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 75140-002-01 identifies a specific commercial package of 166 g in 1 box of Kaydia Patch, labeled by Strong Current Enterprises Limited. This is formulated for use and contains as the active substance.
Is this product currently listed with the FDA?
This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Strong Current Enterprises Limited on May 02, 2020. The current certification is valid through December 31, 2021.
How is this Strong Current Enterprises Limited product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 75140000201. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.