Data / Drug companies / P & L Development, LLC

P & L Development, LLC: 81 products in the FDA NDC directory, labeler code 59726

P & L Development, LLC (labeler code 59726) lists 81 products in the FDA National Drug Code Directory, covering 23 finished drugs by generic name. By type: 68 over the counter drugs, 13 bulk ingredients. Its main marketing category is generic drugs (ANDA). The newest product started marketing on August 15, 2026.

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

59726

Products in commercial distribution

81

Packages

135

Finished drugs by generic name

23

Prescription products

0

Over the counter products

68

Flagged as original packager

64 of 64 products that carry the flag

Started marketing in the last 12 months

6

Products with a marketing end date set

19

Earliest marketing start

March 31, 2016

openFDA record search

api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Products by type

Drugs it lists

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

Dosage forms

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

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