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Data / Drug companies / Burkhart Dental Supply Inc

Burkhart Dental Supply Inc: 28 products in the FDA NDC directory, labeler code 43498

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

Burkhart Dental Supply Inc (labeler code 43498) lists 28 products in the FDA National Drug Code Directory, covering 4 finished drugs by generic name. By type: 16 prescription drugs, 12 over the counter drugs. Its main marketing category is other unapproved drugs. The newest product started marketing on November 4, 2024.

The request: Watch Burkhart Dental Supply Inc (FDA labeler code 43498): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
43498
Products in commercial distribution
28
Packages
28
Finished drugs by generic name
4
Prescription products
16
Over the counter products
12
Flagged as original packager
28 of 28 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
December 14, 2012
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Other unapproved drugs1450%
Over the counter monograph drugs1242.9%
Authorized generics (NDA)27.1%

Products by type

TypeProductsShare
Prescription drugs1657.1%
Over the counter drugs1242.9%

Drugs it lists

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

DrugProductsCompanies listing it
Sodium fluoride12124
Benzocaine10110
Stannous fluoride434
Articaine hydrochloride, epinephrine bitartrate21

Dosage forms

Dosage formProductsShare
Gel2485.7%
Injection, solution27.1%
Concentrate27.1%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Articaine Hydrochloride and Epinephrine43498-993Injection, solutionAuthorized generics (NDA)November 4, 2024
Articaine Hydrochloride and Epinephrine43498-816Injection, solutionAuthorized generics (NDA)November 4, 2024
Burkhart Topical Anesthetic43498-319GelOver the counter monograph drugsNovember 1, 2015
Burkhart Topical Anesthetic43498-318GelOver the counter monograph drugsNovember 1, 2015
Burkhart Topical Anesthetic43498-317GelOver the counter monograph drugsNovember 1, 2015
Burkhart Topical Anesthetic43498-316GelOver the counter monograph drugsNovember 1, 2015
Burkhart Topical Anesthetic43498-315GelOver the counter monograph drugsNovember 1, 2015
Burkhart Topical Anesthetic43498-314GelOver the counter monograph drugsNovember 1, 2015
Burkhart Topical Anesthetic43498-313GelOver the counter monograph drugsNovember 1, 2015
Burkhart Topical Anesthetic43498-312GelOver the counter monograph drugsNovember 1, 2015
Burkhart Topical Anesthetic43498-311GelOver the counter monograph drugsNovember 1, 2015
Burkhart Topical Anesthetic43498-310GelOver the counter monograph drugsNovember 1, 2015
Burkhart43498-201ConcentrateOther unapproved drugsFebruary 1, 2013
Burkhart43498-200ConcentrateOther unapproved drugsFebruary 1, 2013
Burkhart43498-251GelOver the counter monograph drugsJanuary 5, 2013
Burkhart43498-250GelOver the counter monograph drugsJanuary 5, 2013
Burkhart Neutral pH43498-151GelOther unapproved drugsDecember 14, 2012
Burkhart Neutral pH43498-150GelOther unapproved drugsDecember 14, 2012
Burkhart43498-109GelOther unapproved drugsDecember 14, 2012
Burkhart43498-108GelOther unapproved drugsDecember 14, 2012
Burkhart43498-107GelOther unapproved drugsDecember 14, 2012
Burkhart43498-106GelOther unapproved drugsDecember 14, 2012
Burkhart43498-105GelOther unapproved drugsDecember 14, 2012
Burkhart43498-104GelOther unapproved drugsDecember 14, 2012
Burkhart43498-103GelOther unapproved drugsDecember 14, 2012

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.