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Data / Drug companies / Lander Enterprises, LLC

Lander Enterprises, LLC: 10 products in the FDA NDC directory, labeler code 82913

Lander Enterprises, LLC (labeler code 82913) lists 10 products in the FDA National Drug Code Directory, covering 1 finished drug by generic name. By type: 10 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on August 7, 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
82913
Products in commercial distribution
10
Packages
10
Finished drugs by generic name
1
Prescription products
0
Over the counter products
10
Flagged as original packager
10 of 10 products that carry the flag
Started marketing in the last 12 months
6
Earliest marketing start
August 1, 2022
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Over the counter monograph drugs10100%

Products by type

TypeProductsShare
Over the counter drugs10100%

Drugs it lists

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

DrugProductsCompanies listing it
Sodium fluoride10124

Dosage forms

Dosage formProductsShare
Liquid880%
Gel220%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
AutoBrush Mint82913-011LiquidOver the counter monograph drugsAugust 7, 2026
AutoBrush kids watermelon82913-010LiquidOver the counter monograph drugsAugust 7, 2026
AutoBrush kids strawberry82913-009LiquidOver the counter monograph drugsAugust 7, 2026
AutoBrush kids bubblegum82913-008LiquidOver the counter monograph drugsAugust 7, 2026
AutoBrush Mint82913-006GelOver the counter monograph drugsJanuary 1, 2026
AutoBrush bubblegum82913-005GelOver the counter monograph drugsJanuary 1, 2026
AutoBrush Mint82913-004LiquidOver the counter monograph drugsDecember 1, 2022
AutoBrush Watermelon82913-003LiquidOver the counter monograph drugsDecember 1, 2022
AutoBrush strawberry82913-002LiquidOver the counter monograph drugsAugust 1, 2022
AutoBrush Bubblegum82913-001LiquidOver the counter monograph drugsAugust 1, 2022

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.