Tazarotene Cream
NDC Package 51672-1373-2
Package Information
Tazarotene cream is tazarotene is used to treat psoriasis or acne. This formulation utilizes a cream delivery system. Marketed by Sun Pharmaceutical Industries, Inc., this product is identified by NDC 51672-1373 and is authorized under FDA application ANDA208258.
Identification & Billing
- RxCUI: 313200 - tazarotene 0.1 % Topical Cream
- RxCUI: 313200 - tazarotene 1 MG/ML Topical Cream
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 51672 - Sun Pharmaceutical Industries, Inc.
- 51672-1373 - Tazarotene
- 51672-1373-2 - 1 TUBE in 1 CARTON / 30 g in 1 TUBE
- 51672-1373 - Tazarotene
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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Other Available Packages
The following commercial packages are registered under the same Product NDC (51672-1373). 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 51672-1373-2 identifies a specific commercial package of 1 tube in 1 carton / 30 g in 1 tube of Tazarotene, a human prescription drug labeled by Sun Pharmaceutical Industries, Inc.. This cream is formulated for topical use and contains tazarotene 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 Sun Pharmaceutical Industries, Inc. on April 03, 2017. The current certification is valid through December 31, 2026.
What are the primary indications for this medication?
Tazarotene is used to treat psoriasis or acne. It is a retinoid product related to Vitamin A. It works by affecting the growth of skin cells. The foam and lotion forms of this medication are only approved for use on acne.
How is this Sun Pharmaceutical Industries, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 51672137302. Quantities are measured in per "gm or gram", products billed per gram are products measured by weight.. 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 Package segment to maintain the 5-4-2 structure.