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Data / Drug companies / Apozeal Pharmaceuticals Inc

Apozeal Pharmaceuticals Inc: 7 products in the FDA NDC directory, labeler code 83745

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

Apozeal Pharmaceuticals Inc (labeler code 83745) lists 7 products in the FDA National Drug Code Directory, covering 6 finished drugs by generic name. By type: 6 prescription drugs, 1 over the counter drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on November 10, 2025.

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Labeler code
83745
Products in commercial distribution
7
Packages
17
Finished drugs by generic name
6
Prescription products
6
Over the counter products
1
Flagged as original packager
7 of 7 products that carry the flag
Started marketing in the last 12 months
1
Earliest marketing start
July 16, 2024
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)7100%

Products by type

TypeProductsShare
Prescription drugs685.7%
Over the counter drugs114.3%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Solution7100%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Aminocaproic Acid83745-294SolutionGeneric drugs (ANDA)November 10, 2025
Risperidone83745-186SolutionGeneric drugs (ANDA)January 31, 2025
Cetrizine Hydrochloride83745-188SolutionGeneric drugs (ANDA)January 1, 2025
Lactulose83745-405SolutionGeneric drugs (ANDA)December 20, 2024
Lactulose83745-249SolutionGeneric drugs (ANDA)December 20, 2024
Cetirizine Hydrochloride Oral Solution83745-185SolutionGeneric drugs (ANDA)December 20, 2024
Hydroxyzine hydrochloride83745-232SolutionGeneric drugs (ANDA)July 16, 2024

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.