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Data / Drug companies / Niagara Pharmaceuticals Inc.

Niagara Pharmaceuticals Inc.: 7 products in the FDA NDC directory, labeler code 65785

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

Niagara Pharmaceuticals Inc. (labeler code 65785) lists 7 products in the FDA National Drug Code Directory, covering 3 finished drugs by generic name. By type: 7 over the counter drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on April 1, 2024.

The request: Watch Niagara Pharmaceuticals Inc. (FDA labeler code 65785): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
65785
Products in commercial distribution
7
Packages
13
Finished drugs by generic name
3
Prescription products
0
Over the counter products
7
Flagged as original packager
7 of 7 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
September 12, 2011
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)685.7%
Over the counter monograph drugs114.3%

Products by type

TypeProductsShare
Over the counter drugs7100%

Drugs it lists

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

DrugProductsCompanies listing it
Water440
Eyewash26
Chlorhexidine gluconate and propylene glycol13

Dosage forms

Dosage formProductsShare
Solution685.7%
Liquid114.3%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
ULINE Eyewash65785-125SolutionNew drug applications (NDA)April 1, 2024
Pur-Wash65785-168SolutionNew drug applications (NDA)January 30, 2015
Pur-wash65785-166SolutionNew drug applications (NDA)May 24, 2013
Eyewash Station Additive Concentrate65785-034LiquidOver the counter monograph drugsNovember 15, 2011
Pur-wash65785-169SolutionNew drug applications (NDA)September 12, 2011
Pur-wash65785-162SolutionNew drug applications (NDA)September 12, 2011
Pur-wash65785-160SolutionNew drug applications (NDA)September 12, 2011

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.