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Data / Drug companies / Aarkish Pharmaceuticals NJ Inc.

Aarkish Pharmaceuticals NJ Inc.: 9 products in the FDA NDC directory, labeler code 81005

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

Aarkish Pharmaceuticals NJ Inc. (labeler code 81005) lists 9 products in the FDA National Drug Code Directory, covering 6 finished drugs by generic name. By type: 6 prescription drugs, 3 over the counter drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on July 1, 2026.

The request: Watch Aarkish Pharmaceuticals NJ Inc. (FDA labeler code 81005): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
81005
Products in commercial distribution
9
Packages
17
Finished drugs by generic name
6
Prescription products
6
Over the counter products
3
Controlled substance products
Schedule III 1
Flagged as original packager
9 of 9 products that carry the flag
Started marketing in the last 12 months
3
Earliest marketing start
August 15, 2023
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)666.7%
Over the counter monograph drugs333.3%

Products by type

TypeProductsShare
Prescription drugs666.7%
Over the counter drugs333.3%

Drugs it lists

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

DrugProductsCompanies listing it
Metolazone322
Acetazolamide237
Sennosides 8.6 mg tablets11
Butalbital and acetaminophen19
Docusate sodium 50 mg sennosides 8.6 mg11
Aspirin1134

Dosage forms

Dosage formProductsShare
Tablet777.8%
Tablet, film coated111.1%
Tablet, coated111.1%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Senna-S81005-102Tablet, film coatedOver the counter monograph drugsJuly 1, 2026
Senna81005-101TabletOver the counter monograph drugsJuly 1, 2026
Aspirin81005-103Tablet, coatedOver the counter monograph drugsMarch 18, 2026
Butalbital and acetaminophen81005-123TabletGeneric drugs (ANDA)December 3, 2024
Acetazolamide81005-105TabletGeneric drugs (ANDA)December 3, 2024
Acetazolamide81005-104TabletGeneric drugs (ANDA)December 3, 2024
Metolazone81005-126TabletGeneric drugs (ANDA)August 15, 2023
Metolazone81005-125TabletGeneric drugs (ANDA)August 15, 2023
Metolazone81005-124TabletGeneric drugs (ANDA)August 15, 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.