Supres A
NDC Package 65852-014-01
Package Information
Supres A is a . Marketed by Dextrum Laboratories, Inc, this product is identified by NDC 65852-014 and is authorized under FDA application M012.
Identification & Billing
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 65852 - Dextrum Laboratories, Inc
- 65852-014 - Supres A
- 65852-014-01 - 1 BOTTLE, PLASTIC in 1 CARTON / 30 mL in 1 BOTTLE, PLASTIC
- 65852-014 - Supres A
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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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 65852-014-01 identifies a specific commercial package of 1 bottle, plastic in 1 carton / 30 ml in 1 bottle, plastic of Supres A, labeled by Dextrum Laboratories, 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 Dextrum Laboratories, Inc on August 01, 2012. The current certification is valid through October 06, 2025.
How is this Dextrum Laboratories, Inc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 65852001401. 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.