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Data / Drug companies / DXM Pharmacuetical, Inc.

DXM Pharmacuetical, Inc.: 5 products in the FDA NDC directory, labeler code 71598

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

DXM Pharmacuetical, Inc. (labeler code 71598) lists 5 products in the FDA National Drug Code Directory, covering 3 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 September 10, 2024.

The request: Watch DXM Pharmacuetical, Inc. (FDA labeler code 71598): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
71598
Products in commercial distribution
5
Packages
5
Finished drugs by generic name
3
Prescription products
0
Over the counter products
5
Started marketing in the last 12 months
0
Earliest marketing start
October 15, 2020
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 drugs5100%

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
Tablet480%
Liquid120%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Dextabs71598-152TabletOver the counter monograph drugsSeptember 10, 2024
BupropiDex71598-200TabletOver the counter monograph drugsDecember 1, 2023
RoboCough71598-102LiquidOver the counter monograph drugsOctober 1, 2023
RoboHBr Cough SUPPRESSANT71598-100TabletOver the counter monograph drugsMay 31, 2022
RoboTablets71598-015TabletOver the counter monograph drugsOctober 15, 2020

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.