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Data / Drug companies / Acertis Pharmaceuticals, LLC

Acertis Pharmaceuticals, LLC: 5 products in the FDA NDC directory, labeler code 72989

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

Acertis Pharmaceuticals, LLC (labeler code 72989) lists 5 products in the FDA National Drug Code Directory, covering 4 finished drugs by generic name. By type: 5 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on July 14, 2025.

The request: Watch Acertis Pharmaceuticals, LLC (FDA labeler code 72989): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
72989
Products in commercial distribution
5
Packages
6
Finished drugs by generic name
4
Prescription products
5
Over the counter products
0
Controlled substance products
Schedule II 1, Schedule III 1
Flagged as original packager
3 of 3 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
September 1, 2020
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
New drug applications (NDA)480%
Generic drugs (ANDA)120%

Products by type

TypeProductsShare
Prescription drugs5100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Capsule240%
Capsule, extended release120%
Tablet120%
System120%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Levorphanol Tartrate72989-417TabletGeneric drugs (ANDA)July 14, 2025
Phendimetrazine tartrate72989-409Capsule, extended releaseNew drug applications (NDA)November 1, 2022
Prometrium72989-373CapsuleNew drug applications (NDA)November 1, 2022
Prometrium72989-372CapsuleNew drug applications (NDA)November 1, 2022
Licart72989-458SystemNew drug applications (NDA)September 1, 2020

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.