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Data / Drug companies / Septodont, Inc.

Septodont, Inc.: 15 products in the FDA NDC directory, labeler code 0362

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

Septodont, Inc. (labeler code 0362) lists 15 products in the FDA National Drug Code Directory, covering 8 finished drugs by generic name. By type: 15 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on March 19, 2026.

The request: Watch Septodont, Inc. (FDA labeler code 0362): 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
0362
Products in commercial distribution
15
Packages
15
Finished drugs by generic name
8
Prescription products
15
Over the counter products
0
Flagged as original packager
15 of 15 products that carry the flag
Started marketing in the last 12 months
1
Earliest marketing start
January 12, 2011
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)1066.7%
New drug applications (NDA)426.7%
Authorized generics (NDA)16.7%

Products by type

TypeProductsShare
Prescription drugs15100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Injection, solution1386.7%
Solution16.7%
Ointment16.7%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Flavalta0362-1200Injection, solutionNew drug applications (NDA)March 19, 2026
DycloPro0362-3971SolutionGeneric drugs (ANDA)September 1, 2019
Zorcaine0362-0830Injection, solutionAuthorized generics (NDA)April 5, 2019
Lidocaine0362-0262Injection, solutionGeneric drugs (ANDA)August 10, 2018
Lidocaine0362-0898Injection, solutionGeneric drugs (ANDA)July 18, 2018
Carbocaine0362-0753Injection, solutionGeneric drugs (ANDA)June 21, 2018
Marcaine0362-0557Injection, solutionGeneric drugs (ANDA)June 12, 2018
Scandonest 3% Plain0362-1098Injection, solutionGeneric drugs (ANDA)December 22, 2017
Lignospan Forte0362-1096Injection, solutionGeneric drugs (ANDA)December 1, 2017
Lignospan Standard0362-1095Injection, solutionGeneric drugs (ANDA)November 28, 2017
Lidocaine0362-0221OintmentGeneric drugs (ANDA)May 20, 2015
Vivacaine0362-9011Injection, solutionGeneric drugs (ANDA)June 1, 2013
Oraverse0362-0101Injection, solutionNew drug applications (NDA)June 1, 2011
Septocaine and Epinephrine0362-9049Injection, solutionNew drug applications (NDA)January 12, 2011
Septocaine and Epinephrine0362-9048Injection, solutionNew drug applications (NDA)January 12, 2011

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.