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Data / Drug companies / Carnegie Pharmaceuticals LLC

Carnegie Pharmaceuticals LLC: 17 products in the FDA NDC directory, labeler code 80005

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

Carnegie Pharmaceuticals LLC (labeler code 80005) lists 17 products in the FDA National Drug Code Directory, covering 10 finished drugs by generic name. By type: 17 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on June 30, 2026.

The request: Watch Carnegie Pharmaceuticals LLC (FDA labeler code 80005): 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
80005
Products in commercial distribution
17
Packages
27
Finished drugs by generic name
10
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
7
Earliest marketing start
March 15, 2021
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)17100%

Products by type

TypeProductsShare
Prescription drugs17100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Tablet847.1%
Capsule423.5%
Solution211.8%
Tablet, film coated211.8%
Powder, for suspension15.9%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Letrozole80005-139Tablet, film coatedGeneric drugs (ANDA)June 30, 2026
Vigabatrin80005-167Tablet, film coatedGeneric drugs (ANDA)February 18, 2026
Rasagiline80005-142TabletGeneric drugs (ANDA)January 15, 2026
Rasagiline80005-141TabletGeneric drugs (ANDA)January 15, 2026
Lomustine80005-116CapsuleGeneric drugs (ANDA)November 10, 2025
Lomustine80005-115CapsuleGeneric drugs (ANDA)November 10, 2025
Lomustine80005-114CapsuleGeneric drugs (ANDA)November 10, 2025
Balsalazide disodium80005-126CapsuleGeneric drugs (ANDA)June 30, 2025
Clindamycin Phosphate80005-131SolutionGeneric drugs (ANDA)June 16, 2025
Primidone80005-118TabletGeneric drugs (ANDA)May 1, 2024
Primidone80005-117TabletGeneric drugs (ANDA)May 1, 2024
Famotidine80005-119Powder, for suspensionGeneric drugs (ANDA)August 10, 2023
Etravirine80005-113TabletGeneric drugs (ANDA)June 7, 2022
Etravirine80005-112TabletGeneric drugs (ANDA)June 7, 2022
Aminocaproic acid80005-130SolutionGeneric drugs (ANDA)March 18, 2021
Aminocaproic acid80005-129TabletGeneric drugs (ANDA)March 15, 2021
Aminocaproic acid80005-128TabletGeneric drugs (ANDA)March 15, 2021

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.