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Data / Drug companies / Dextrum Laboratories, Inc

Dextrum Laboratories, Inc: 21 products in the FDA NDC directory, labeler code 65852

Dextrum Laboratories, Inc (labeler code 65852) lists 21 products in the FDA National Drug Code Directory, covering 9 finished drugs by generic name. By type: 21 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on April 11, 2024.

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
65852
Products in commercial distribution
21
Packages
21
Finished drugs by generic name
9
Prescription products
0
Over the counter products
21
Flagged as original packager
21 of 21 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
September 1, 2004
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 drugs21100%

Products by type

TypeProductsShare
Over the counter drugs21100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Solution1152.4%
Liquid628.6%
Syrup29.5%
Spray29.5%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Giltuss D65852-010SyrupOver the counter monograph drugsApril 11, 2024
Rompe Pecho CF65852-013LiquidOver the counter monograph drugsOctober 1, 2023
IceQuake Lidocaine Analgesic65852-026LiquidOver the counter monograph drugsAugust 1, 2022
Childrens Giltuss EX Expectorant65852-016SolutionOver the counter monograph drugsJune 22, 2020
Giltuss EX Expectorant65852-008SolutionOver the counter monograph drugsJune 22, 2020
Childrens Giltuss Honey DM Cough65852-007LiquidOver the counter monograph drugsJune 22, 2020
Giltuss Honey Cough and Chest Congestion65852-005LiquidOver the counter monograph drugsJune 22, 2020
Giltuss Honey DM Cough65852-004SolutionOver the counter monograph drugsJune 22, 2020
Childrens Giltuss Honey Cough and Chest Congestion65852-003SolutionOver the counter monograph drugsJune 22, 2020
Giltuss HBP Cough and Chest Congestion65852-006SolutionOver the counter monograph drugsNovember 13, 2018
Giltuss Childrens Allergy Plus65852-018SolutionOver the counter monograph drugsNovember 7, 2018
Giltuss Childrens Cough and Cold65852-011SolutionOver the counter monograph drugsNovember 7, 2018
Giltuss Diabetic65852-009SolutionOver the counter monograph drugsOctober 17, 2018
Giltuss Childrens Cough and Chest Congestion65852-019SolutionOver the counter monograph drugsOctober 2, 2018
Giltuss Allergy Plus65852-017SolutionOver the counter monograph drugsOctober 2, 2018
Giltuss Cough and Cold65852-012SolutionOver the counter monograph drugsOctober 2, 2018
Giltuss Bucalsep65852-015SprayOver the counter monograph drugsJuly 26, 2018
Dometuss65852-002LiquidOver the counter monograph drugsJanuary 21, 2016
Supress a65852-020SyrupOver the counter monograph drugsAugust 1, 2012
Rycontuss65852-021LiquidOver the counter monograph drugsMay 31, 2011
Finafta MultiOral65852-001SprayOver the counter monograph drugsSeptember 1, 2004

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