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Data / Drug companies / Coating Place, LLC

Coating Place, LLC: 10 products in the FDA NDC directory, labeler code 81842

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

Coating Place, LLC (labeler code 81842) lists 10 products in the FDA National Drug Code Directory. By type: 10 drugs for further processing. Its main marketing category is drugs for further processing. The newest product started marketing on May 20, 2019.

The request: Watch Coating Place, LLC (FDA labeler code 81842): each new product listing and each discontinued product. $10 of work on sign-up, no card.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Labeler code
81842
Products in commercial distribution
10
Packages
10
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Controlled substance products
Schedule II 5
Started marketing in the last 12 months
0
Earliest marketing start
June 8, 1994
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Drugs for further processing10100%

Products by type

TypeProductsShare
Drugs for further processing10100%

Dosage forms

Dosage formProductsShare
Capsule, extended release550%
Granule330%
Granule, delayed release220%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Methylphenidate hcl81842-749Capsule, extended releaseDrugs for further processingMay 20, 2019
Methylphenidate hcl81842-349Capsule, extended releaseDrugs for further processingMay 20, 2019
Methylphenidate hcl81842-249Capsule, extended releaseDrugs for further processingMay 20, 2019
Methylphenidate hcl81842-149Capsule, extended releaseDrugs for further processingMay 20, 2019
Methylphenidate hcl81842-049Capsule, extended releaseDrugs for further processingMay 20, 2019
Famotidine81842-604GranuleDrugs for further processingMarch 16, 2007
Omeprazole81842-791Granule, delayed releaseDrugs for further processingJuly 14, 2003
Potassium chloride81842-353GranuleDrugs for further processingNovember 28, 1998
Aminosalicylic acid granules81842-467Granule, delayed releaseDrugs for further processingFebruary 15, 1995
Acetaminophen81842-418GranuleDrugs for further processingJune 8, 1994

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.