Skip to the page

Data / Drug companies / Long Grove Pharmaceuticals, LLC

Long Grove Pharmaceuticals, LLC: 14 products in the FDA NDC directory, labeler code 81298

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

Long Grove Pharmaceuticals, LLC (labeler code 81298) lists 14 products in the FDA National Drug Code Directory, covering 9 finished drugs by generic name. By type: 14 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on March 3, 2026.

The request: Watch Long Grove Pharmaceuticals, LLC (FDA labeler code 81298): 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
81298
Products in commercial distribution
14
Packages
15
Finished drugs by generic name
9
Prescription products
14
Over the counter products
0
Controlled substance products
Schedule II 1
Flagged as original packager
14 of 14 products that carry the flag
Started marketing in the last 12 months
1
Earliest marketing start
May 2, 2022
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)857.1%
New drug applications (NDA)642.9%

Products by type

TypeProductsShare
Prescription drugs14100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Solution750%
Suspension321.4%
Injection321.4%
Injection, powder, for solution17.1%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Dalbavancin81298-2390Injection, powder, for solutionGeneric drugs (ANDA)March 3, 2026
Methadone Hydrochloride81298-7500InjectionGeneric drugs (ANDA)June 28, 2025
Sodium bicarbonate81298-7620SolutionGeneric drugs (ANDA)September 30, 2024
Ak-fluor81298-8660InjectionNew drug applications (NDA)September 28, 2024
Eribulin Mesylate81298-3890SolutionGeneric drugs (ANDA)July 22, 2024
Vasopressin in 0.9% Sodium Chloride81298-8554SolutionNew drug applications (NDA)July 12, 2024
Vasopressin in 0.9% Sodium Chloride81298-8552SolutionNew drug applications (NDA)July 12, 2024
Norepinephrine81298-9659SolutionNew drug applications (NDA)February 2, 2024
Norepinephrine81298-9658SolutionNew drug applications (NDA)February 2, 2024
Norepinephrine81298-9655SolutionNew drug applications (NDA)February 2, 2024
Carboprost Tromethamine81298-5010InjectionGeneric drugs (ANDA)October 15, 2022
Triamcinolone Acetonide81298-5785SuspensionGeneric drugs (ANDA)May 2, 2022
Triamcinolone Acetonide81298-5783SuspensionGeneric drugs (ANDA)May 2, 2022
Triamcinolone Acetonide81298-5781SuspensionGeneric drugs (ANDA)May 2, 2022

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.