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Data / Drug companies / GVS TM Inc

GVS TM Inc: 17 products in the FDA NDC directory, labeler code 87069

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

GVS TM Inc (labeler code 87069) lists 17 products in the FDA National Drug Code Directory, covering 5 finished drugs by generic name. By type: 17 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on June 24, 2026.

The request: Watch GVS TM Inc (FDA labeler code 87069): each new product listing and each discontinued product. $10 of work on sign-up, no card.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Labeler code
87069
Products in commercial distribution
17
Packages
17
Finished drugs by generic name
5
Prescription products
17
Over the counter products
0
Flagged as original packager
17 of 17 products that carry the flag
Started marketing in the last 12 months
14
Earliest marketing start
September 15, 2025
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
New drug applications (NDA)17100%

Products by type

TypeProductsShare
Prescription drugs17100%

Drugs it lists

Finished drugs by generic name, with how many companies list each.

DrugProductsCompanies listing it
Cp2d/as-3 anticoagulant and additive system81
Cp2d/as-3 - anticoagulant and additive system21
As-321
Cp2d11
Cp2d/as-3 triple with sampling system11

Dosage forms

Dosage formProductsShare
Solution17100%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Leukotrap WB System87069-736SolutionNew drug applications (NDA)June 24, 2026
Leukotrap WB system - CP2D87069-726SolutionNew drug applications (NDA)June 24, 2026
Leukotrap WB System87069-136SolutionNew drug applications (NDA)June 24, 2026
Leukotrap WB System87069-136SolutionNew drug applications (NDA)June 24, 2026
Leukotrap RC System87069-129SolutionNew drug applications (NDA)June 23, 2026
Leukotrap RC System87069-129SolutionNew drug applications (NDA)June 23, 2026
Leukotrap WB System - CP2D87069-126SolutionNew drug applications (NDA)June 23, 2026
Leukotrap RC PL System87069-123SolutionNew drug applications (NDA)June 23, 2026
Leukotrap RC PL System87069-123SolutionNew drug applications (NDA)June 23, 2026
Leukotrap RC PL System87069-123SolutionNew drug applications (NDA)June 23, 2026
Blood Collection System87069-121SolutionNew drug applications (NDA)June 23, 2026
Leukotrap WB system - CP2D87069-726SolutionNew drug applications (NDA)June 2, 2026
Leukotrap RC System87069-129SolutionNew drug applications (NDA)March 2, 2026
Leukotrap WB System - CP2D87069-126SolutionNew drug applications (NDA)November 28, 2025
Cp2d87069-455SolutionNew drug applications (NDA)September 30, 2025
As-387069-462SolutionNew drug applications (NDA)September 15, 2025
As-387069-460SolutionNew drug applications (NDA)September 15, 2025

CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.