Tamoxifen Citrate Tablet, Film Coated
NDC Package 75907-059-30
Package Information
Tamoxifen Citrate tablets is tamoxifen is used to treat breast cancer. This formulation utilizes a tablet, film coated delivery system. Marketed by Dr. Reddy's Labratories Inc., this product is identified by NDC 75907-059 and is authorized under FDA application ANDA075797.
Identification & Billing
- RxCUI: 198240 - tamoxifen citrate 10 MG Oral Tablet
- RxCUI: 198240 - tamoxifen 10 MG Oral Tablet
- RxCUI: 198240 - tamoxifen 10 MG (as tamoxifen citrate 15.2 MG) Oral Tablet
- RxCUI: 313195 - tamoxifen citrate 20 MG Oral Tablet
- RxCUI: 313195 - tamoxifen 20 MG Oral Tablet
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 75907 - Dr. Reddy's Labratories Inc.
- 75907-059 - Tamoxifen Citrate
- 75907-059-30 - 30 TABLET, FILM COATED in 1 BOTTLE
- 75907-059 - Tamoxifen Citrate
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.
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.
Other Available Packages
The following commercial packages are registered under the same Product NDC (75907-059). 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 75907-059-30 identifies a specific commercial package of 30 tablet, film coated in 1 bottle of Tamoxifen Citrate, a human prescription drug labeled by Dr. Reddy's Labratories Inc.. This tablet, film coated is formulated for oral use and contains tamoxifen citrate 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 Dr. Reddy's Labratories Inc. on August 22, 2024. The current certification is valid through December 31, 2026.
What are the primary indications for this medication?
Tamoxifen is used to treat breast cancer. It is also used to reduce the chances of breast cancer in high-risk patients. This medication can block the growth of breast cancer. It works by interfering with the effects of estrogen in the breast tissue.
How is this Dr. Reddy's Labratories Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 75907005930. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 30 total billable units per package. 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.