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Data / Drug companies / Hisamitsu America, Inc.

Hisamitsu America, Inc.: 5 products in the FDA NDC directory, labeler code 55328

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

Hisamitsu America, Inc. (labeler code 55328) lists 5 products in the FDA National Drug Code Directory, covering 4 finished drugs by generic name. By type: 5 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on January 1, 2026.

The request: Watch Hisamitsu America, Inc. (FDA labeler code 55328): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
55328
Products in commercial distribution
5
Packages
9
Finished drugs by generic name
4
Prescription products
0
Over the counter products
5
Flagged as original packager
5 of 5 products that carry the flag
Started marketing in the last 12 months
1
Earliest marketing start
June 1, 2013
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Over the counter monograph drugs480%
Generic drugs (ANDA)120%

Products by type

TypeProductsShare
Over the counter drugs5100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Gel240%
Cream120%
Patch120%
Liquid120%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Salonpas LIDOCAINE Pain Relieving55328-100PatchOver the counter monograph drugsJanuary 1, 2026
Salonpas LIDOCAINE PLUS55328-901LiquidOver the counter monograph drugsSeptember 1, 2017
Salonpas LIDOCAINE PLUS55328-902CreamOver the counter monograph drugsJune 23, 2017
Salonpas55328-801GelGeneric drugs (ANDA)March 21, 2016
Salonpas DEEP Relieving55328-900GelOver the counter monograph drugsJune 1, 2013

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.