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Data / Drug companies / Jvet Pharmaceuticals LLC

Jvet Pharmaceuticals LLC: 7 products in the FDA NDC directory, labeler code 86211

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

Jvet Pharmaceuticals LLC (labeler code 86211) lists 7 products in the FDA National Drug Code Directory, covering 7 finished drugs by generic name. By type: 7 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on May 22, 2026.

The request: Watch Jvet Pharmaceuticals LLC (FDA labeler code 86211): 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
86211
Products in commercial distribution
7
Packages
7
Finished drugs by generic name
7
Prescription products
7
Over the counter products
0
Controlled substance products
Schedule IV 1
Flagged as original packager
7 of 7 products that carry the flag
Started marketing in the last 12 months
6
Earliest marketing start
October 21, 2025
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)7100%

Products by type

TypeProductsShare
Prescription drugs7100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Injection342.9%
Solution114.3%
Solution/ drops114.3%
Injection, solution114.3%
Injection, powder, lyophilized, for solution114.3%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Methocarbamol86211-114InjectionGeneric drugs (ANDA)May 22, 2026
Ondansetron86211-115InjectionGeneric drugs (ANDA)March 23, 2026
Doxycycline86211-116Injection, powder, lyophilized, for solutionGeneric drugs (ANDA)January 27, 2026
Tobramycin86211-110Solution/ dropsGeneric drugs (ANDA)January 26, 2026
Glycopyrrolate86211-113InjectionGeneric drugs (ANDA)December 31, 2025
Gabapentin86211-112SolutionGeneric drugs (ANDA)December 15, 2025
Midazolam Hydrochloride86211-111Injection, solutionGeneric drugs (ANDA)October 21, 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.