Marvona-25 Suik Injection, Solution
NDC Package 87063-079-01
Package Information
Marvona-25 Suik (bupivacaine hydrochloride) injection is bupivacaine Hydrochloride Injection is indicated in adults for the production of local or regional anesthesia or analgesia for surgery, dental and oral surgery procedures, diagnostic and therapeutic procedures, and for obstetrical procedures. This formulation utilizes a injection, solution delivery system. Marketed by Asclemed Usa, Inc., this product is identified by NDC 87063-079.
Identification & Billing
Clinical Specifications
- Epidural - Administration upon or over the dura mater.
- Infiltration - Administration that results in substances passing into tissue spaces or into cells.
- Intracaudal - Administration within the cauda equina.
- Perineural - Administration surrounding a nerve or nerves.
Regulatory & Marketing
Hierarchy Structure
- 87063 - Asclemed Usa, Inc.
- 87063-079 - Marvona-25 Suik
- 87063-079-01 - 1 VIAL, SINGLE-DOSE in 1 CARTON / 10 mL in 1 VIAL, SINGLE-DOSE
- 87063-079 - Marvona-25 Suik
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 87063-079-01 identifies a specific commercial package of 1 vial, single-dose in 1 carton / 10 ml in 1 vial, single-dose of Marvona-25 Suik, a human prescription drug labeled by Asclemed Usa, Inc.. This product is billed for "EA" each discreet unit and contains an estimated amount of 1 billable units per package. This injection, solution is formulated for epidural; infiltration; intracaudal; perineural use and contains bupivacaine hydrochloride 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 Asclemed Usa, Inc. on January 24, 2026. The current certification is valid through December 31, 2027.
How is this Asclemed Usa, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 87063007901. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 1 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.