Cyclosporine Solution
NDC Package 0172-7313-20
Package Information
Cyclosporine solution is cyclosporine is used to prevent organ rejection in people who have received a liver, kidney, or heart transplant. This formulation utilizes a solution delivery system. Marketed by Teva Pharmaceuticals Usa, Inc., this product is identified by NDC 0172-7313 and is authorized under FDA application ANDA065078.
Identification & Billing
- RxCUI: 835886 - cycloSPORINE, modified 100 MG/mL Oral Solution
- RxCUI: 835886 - cyclosporine, modified 100 MG/ML Oral Solution
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 0172 - Teva Pharmaceuticals Usa, Inc.
- 0172-7313 - Cyclosporine
- 0172-7313-20 - 1 BOTTLE in 1 PACKAGE / 50 mL in 1 BOTTLE
- 0172-7313 - Cyclosporine
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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Billing & HCPCS Mapping
To facilitate insurance claims and reimbursement, this drug package is mapped to specific HCPCS administrative codes. This crosswalk aligns clinical data with the billing standards used in ASP (Average Sales Price), AWP, and OPPS payment systems. Use the cards below to identify the correct billable units for provider claims.
Note for Medical Coders: These mappings are synthesized from various CMS datasets including OPPS, PrEP, and DAC (Data Analysis and Coding) contractors. Always confirm unit conversions against the current quarter's pricing files before final submission.
* 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 0172-7313-20 identifies a specific commercial package of 1 bottle in 1 package / 50 ml in 1 bottle of Cyclosporine, a human prescription drug labeled by Teva Pharmaceuticals Usa, Inc.. This solution is formulated for oral use and contains cyclosporine as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Teva Pharmaceuticals Usa, Inc. on March 29, 2005. The current certification is valid through December 31, 2026.
What are the primary indications for this medication?
Cyclosporine is used to prevent organ rejection in people who have received a liver, kidney, or heart transplant. It is usually taken along with other medications to allow your new organ to function normally. Cyclosporine belongs to a class of drugs known as immunosuppressants. It works by weakening the immune system to help your body accept the new organ as if it were your own.
How is this Teva Pharmaceuticals Usa, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 00172731320. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. 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 Labeler segment to maintain the 5-4-2 structure.