Clindamycin Phosphate Solution
NDC Package 51672-4081-4
Package Information
Clindamycin Phosphate solution is a medication used to treat acne. This formulation utilizes a solution delivery system. Marketed by Sun Pharmaceutical Industries, Inc., this product is identified by NDC 51672-4081 and is authorized under FDA application ANDA065184.
Identification & Billing
- RxCUI: 309333 - clindamycin phosphate 1 % Topical Solution
- RxCUI: 309333 - clindamycin 10 MG/ML Topical Solution
- RxCUI: 309333 - clindamycin (as clindamycin phosphate) 1 % Topical Solution
- RxCUI: 309333 - clindamycin 1 % Topical Solution
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 51672 - Sun Pharmaceutical Industries, Inc.
- 51672-4081 - Clindamycin Phosphate
- 51672-4081-4 - 1 BOTTLE, WITH APPLICATOR in 1 CARTON / 60 mL in 1 BOTTLE, WITH APPLICATOR
- 51672-4081 - Clindamycin Phosphate
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 (51672-4081). 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 51672-4081-4 identifies a specific commercial package of 1 bottle, with applicator in 1 carton / 60 ml in 1 bottle, with applicator of Clindamycin Phosphate, a human prescription drug labeled by Sun Pharmaceutical Industries, Inc.. This solution is formulated for topical use and contains clindamycin phosphate 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 March 31, 2004. The current certification is valid through December 31, 2027.
What are the primary indications for this medication?
This medication is used to treat acne. It helps to decrease the number of acne lesions. Clindamycin is an antibiotic which works by stopping the growth of bacteria.
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: 51672408104. 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 Package segment to maintain the 5-4-2 structure.