Vancomycin Hydrochloride Injection, Powder, Lyophilized, For Solution
NDC Package 87188-202-90
Package Information
Vancomycin Hydrochloride injection is vancomycin hydrochloride for injection is indicated for the treatment of serious or severe infections caused by susceptible strains of methicillin-resistant (β-lactam-resistant) staphylococci. This formulation utilizes a injection, powder, lyophilized, for solution delivery system. Marketed by Plano Pharmaceuticals Inc., this product is identified by NDC 87188-202 and is authorized under FDA application ANDA090250.
Identification & Billing
- RxCUI: 1807513 - vancomycin 1 GM Injection
- RxCUI: 1807513 - vancomycin 1000 MG Injection
- RxCUI: 1807513 - vancomycin (as vancomycin HCl) 1 GM Injection
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 87188 - Plano Pharmaceuticals Inc.
- 87188-202 - Vancomycin Hydrochloride
- 87188-202-90 - 10 VIAL in 1 CARTON / 100 mL in 1 VIAL (87188-202-01)
- 87188-202 - Vancomycin Hydrochloride
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.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 87188-202-90 identifies a specific commercial package of 10 vial in 1 carton / 100 ml in 1 vial (87188-202-01) of Vancomycin Hydrochloride, a human prescription drug labeled by Plano Pharmaceuticals Inc.. This injection, powder, lyophilized, for solution is formulated for intravenous use and contains vancomycin 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 Plano Pharmaceuticals Inc. on April 27, 2010. The current certification is valid through December 31, 2027.
How is this Plano Pharmaceuticals Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 87188020290. 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.