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Data / Drug companies / Wavelength Enterprises LTD

Wavelength Enterprises LTD: 47 products in the FDA NDC directory, labeler code 58175

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

Wavelength Enterprises LTD (labeler code 58175) lists 47 products in the FDA National Drug Code Directory. By type: 47 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on January 12, 2025.

The request: Watch Wavelength Enterprises LTD (FDA labeler code 58175): 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
58175
Products in commercial distribution
47
Packages
48
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Controlled substance products
Schedule IV 4, Schedule V 1
Started marketing in the last 12 months
0
Products with a marketing end date set
1
Earliest marketing start
January 1, 2000
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients47100%

Products by type

TypeProductsShare
Bulk ingredients47100%

Dosage forms

Dosage formProductsShare
Powder4697.9%
Liquid12.1%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Podofilox58175-0664PowderBulk ingredientsJanuary 12, 2025
Ganaxolone58175-0654PowderBulk ingredientsNovember 15, 2023
Clascoterone58175-0650PowderBulk ingredientsDecember 30, 2022
Remimazolam besylate58175-0648PowderBulk ingredientsAugust 31, 2022
D9-tetrahydrocannabinol-naphthoylester58175-0644PowderBulk ingredientsApril 15, 2022
Tapinarof58175-0646PowderBulk ingredientsMarch 15, 2022
Cantharidin58175-0642PowderBulk ingredientsApril 1, 2021
Pralidoxime chloride58175-0640PowderBulk ingredientsFebruary 1, 2021
Sitagliptin phosphate monohydrate58175-0638PowderBulk ingredientsSeptember 1, 2020
Naltrexone hydrochloride58175-0632PowderBulk ingredientsSeptember 1, 2019
Naltrexone base58175-0628PowderBulk ingredientsJune 1, 2019
Umeclidinium bromide58175-0626PowderBulk ingredientsApril 1, 2019
Glycopyrronium bromide58175-0624PowderBulk ingredientsApril 1, 2019
Crisaborole58175-0622PowderBulk ingredientsApril 1, 2019
Sitagliptin phosphate58175-0620PowderBulk ingredientsApril 1, 2019
Sugammadex58175-0618PowderBulk ingredientsAugust 30, 2018
Fexofenadine hydrochloride58175-0616PowderBulk ingredientsNovember 30, 2017
Tavaborole58175-0614PowderBulk ingredientsAugust 15, 2016
Efinaconazole58175-0606PowderBulk ingredientsMay 15, 2015
Permethrin58175-0604LiquidBulk ingredientsMay 15, 2015
Ibrutinib58175-0602PowderBulk ingredientsDecember 30, 2014
Fulvestrant58175-0600PowderBulk ingredientsAugust 1, 2014
Tiotropium bromide58175-0565PowderBulk ingredientsDecember 12, 2011
Rotigotine58175-0545PowderBulk ingredientsJune 7, 2010
Cisatracurium besylate58175-0541PowderBulk ingredientsApril 30, 2010

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.