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Data / Drug companies / Dentsply Pharmaceutical

Dentsply Pharmaceutical: 8 products in the FDA NDC directory, labeler code 66312

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

Dentsply Pharmaceutical (labeler code 66312) lists 8 products in the FDA National Drug Code Directory, covering 6 finished drugs by generic name. By type: 8 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on December 4, 2017.

The request: Watch Dentsply Pharmaceutical (FDA labeler code 66312): 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
66312
Products in commercial distribution
8
Packages
8
Finished drugs by generic name
6
Prescription products
8
Over the counter products
0
Flagged as original packager
8 of 8 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
November 18, 1965
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)562.5%
Authorized generics (NDA)225%
New drug applications (NDA)112.5%

Products by type

TypeProductsShare
Prescription drugs8100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Injection, solution787.5%
Gel112.5%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Citanest Forte DENTAL66312-580Injection, solutionGeneric drugs (ANDA)December 4, 2017
Articadent66312-602Injection, solutionAuthorized generics (NDA)September 1, 2009
Articadent66312-601Injection, solutionAuthorized generics (NDA)September 1, 2009
Oraqix66312-110GelNew drug applications (NDA)January 2, 2004
Xylocaine66312-181Injection, solutionGeneric drugs (ANDA)January 22, 1985
Xylocaine66312-176Injection, solutionGeneric drugs (ANDA)January 22, 1985
Polocaine66312-441Injection, solutionGeneric drugs (ANDA)October 10, 1984
Citanest Plain66312-630Injection, solutionGeneric drugs (ANDA)November 18, 1965

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.