Lidoforte Hemorrhoidal
NDC Package 71890-310-01
Package Information
Lidoforte Hemorrhoidal is a . Marketed by Satius Pharmaceuticals, Llc, this product is identified by NDC 71890-310 and is authorized under FDA application M015.
Identification & Billing
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 71890 - Satius Pharmaceuticals, Llc
- 71890-310 - Lidoforte Hemorrhoidal
- 71890-310-01 - 1 TUBE in 1 BOX / 44.3603 mL in 1 TUBE
- 71890-310 - Lidoforte Hemorrhoidal
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 71890-310-01 identifies a specific commercial package of 1 tube in 1 box / 44.3603 ml in 1 tube of Lidoforte Hemorrhoidal, labeled by Satius Pharmaceuticals, Llc. 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 Satius Pharmaceuticals, Llc on November 18, 2017. The current certification is valid through May 30, 2021.
How is this Satius Pharmaceuticals, Llc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 71890031001. 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.