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Data / Drug companies / Brisk Pharmaceuticals

Brisk Pharmaceuticals: 6 products in the FDA NDC directory, labeler code 73614

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

Brisk Pharmaceuticals (labeler code 73614) lists 6 products in the FDA National Drug Code Directory, covering 6 finished drugs by generic name. By type: 6 prescription drugs. Its main marketing category is other unapproved drugs. The newest product started marketing on February 10, 2025.

The request: Watch Brisk Pharmaceuticals (FDA labeler code 73614): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
73614
Products in commercial distribution
6
Packages
6
Finished drugs by generic name
6
Prescription products
6
Over the counter products
0
Flagged as original packager
3 of 3 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
March 10, 2023
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Other unapproved drugs350%
Generic drugs (ANDA)350%

Products by type

TypeProductsShare
Prescription drugs6100%

Drugs it lists

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

DrugProductsCompanies listing it
Moxifloxacin 0.5%, bromfenac 0.09%, prednisolone acetate 1%11
Clindamycin, ibuprofen, chlorhexidine gluconate11
Ibuprofen1190
Cephalexin, ibuprofen, chlorhexidine gluconate11
Clindamycin hydrochloride134
Chlorhexidine gluconate oral rinse14

Dosage forms

Dosage formProductsShare
Kit350%
Tablet, film coated116.7%
Capsule116.7%
Solution116.7%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
ClindaCare73614-922KitOther unapproved drugsFebruary 10, 2025
Strenza plus73614-732KitOther unapproved drugsFebruary 10, 2025
Orapaz73614-417KitOther unapproved drugsFebruary 10, 2025
Ibuprofen73614-201Tablet, film coatedGeneric drugs (ANDA)May 23, 2024
Chlorhexidine Gluconate Oral Rinse73614-203SolutionGeneric drugs (ANDA)July 27, 2023
Clindamycin Hydrochloride73614-204CapsuleGeneric drugs (ANDA)March 10, 2023

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.