Nystatin And Triamcinolone Acetonide
NDC Package 53002-9360-2
Package Information
Nystatin And Triamcinolone Acetonide is cream and Ointment are indicated for the treatment of cutaneous candidiasis; it has been demonstrated that the nystatin-steroid combination provides greater benefit than the nystatin component alone during the first few days of treatment. Marketed by Rpk Pharmaceuticals, Inc., this product is identified by NDC 53002-9360 and is authorized under FDA application ANDA062364.
Identification & Billing
- RxCUI: 1053753 - nystatin 100,000 UNT/GM / triamcinolone acetonide 1 MG/GM Topical Cream
- RxCUI: 1053753 - nystatin 100000 UNT/ML / triamcinolone acetonide 1 MG/ML Topical Cream
- RxCUI: 1053753 - nystatin 100,000 UNT/ML / triamcinolone acetonide 1 MG/ML Topical Cream
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 53002 - Rpk Pharmaceuticals, Inc.
- 53002-9360 - Nystatin And Triamcinolone Acetonide
- 53002-9360-2 - 30 g in 1 TUBE
- 53002-9360 - Nystatin And Triamcinolone Acetonide
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.
* Please review the full disclaimer at the bottom of this page.
Other Available Packages
The following commercial packages are registered under the same Product NDC (53002-9360). Click a package code to view its specific billing and regulatory data.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 53002-9360-2 identifies a specific commercial package of 30 g in 1 tube of Nystatin And Triamcinolone Acetonide, labeled by Rpk Pharmaceuticals, Inc.. 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 Rpk Pharmaceuticals, Inc. on December 22, 1987. The current certification is valid through December 31, 2024.
How is this Rpk Pharmaceuticals, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 53002936002. 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 Package segment to maintain the 5-4-2 structure.