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Data / Drug companies / Clinical Solutions Wholesale, LLC

Clinical Solutions Wholesale, LLC: 67 products in the FDA NDC directory, labeler code 58118

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

Clinical Solutions Wholesale, LLC (labeler code 58118) lists 67 products in the FDA National Drug Code Directory, covering 14 finished drugs by generic name. By type: 67 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on March 1, 2025.

The request: Watch Clinical Solutions Wholesale, LLC (FDA labeler code 58118): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
58118
Products in commercial distribution
67
Packages
67
Finished drugs by generic name
14
Prescription products
67
Over the counter products
0
Controlled substance products
Schedule III 13, Schedule IV 28, Schedule V 18
Started marketing in the last 12 months
0
Earliest marketing start
September 4, 1985
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)6191%
Other unapproved drugs69%

Products by type

TypeProductsShare
Prescription drugs67100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Tablet4262.7%
Capsule2029.9%
Tablet, film coated46%
Tablet, coated11.5%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Phenobarbital58118-0576TabletOther unapproved drugsMarch 1, 2025
Phenobarbital58118-0574TabletOther unapproved drugsMarch 1, 2025
Phenobarbital58118-0573TabletOther unapproved drugsMarch 1, 2025
Phenobarbital58118-0572TabletOther unapproved drugsMarch 1, 2025
Lorazepam58118-0774TabletGeneric drugs (ANDA)June 25, 2023
Lorazepam58118-0773TabletGeneric drugs (ANDA)June 25, 2023
Pregabalin58118-0765CapsuleGeneric drugs (ANDA)March 29, 2023
Pregabalin58118-0764CapsuleGeneric drugs (ANDA)March 29, 2023
Pregabalin58118-0763CapsuleGeneric drugs (ANDA)March 29, 2023
Pregabalin58118-0762CapsuleGeneric drugs (ANDA)March 29, 2023
Pregabalin58118-0761CapsuleGeneric drugs (ANDA)March 29, 2023
Pregabalin58118-0760CapsuleGeneric drugs (ANDA)March 29, 2023
Pregabalin58118-0759CapsuleGeneric drugs (ANDA)March 29, 2023
Pregabalin58118-0758CapsuleGeneric drugs (ANDA)March 29, 2023
Tramadol Hydrochloride58118-2348Tablet, coatedGeneric drugs (ANDA)February 13, 2023
Phenobarbital58118-1626TabletOther unapproved drugsNovember 30, 2022
Clonazepam58118-0154TabletGeneric drugs (ANDA)April 14, 2022
Clonazepam58118-0153TabletGeneric drugs (ANDA)April 14, 2022
Clonazepam58118-0152TabletGeneric drugs (ANDA)April 14, 2022
Lacosamide58118-8815Tablet, film coatedGeneric drugs (ANDA)March 17, 2022
Lacosamide58118-8814Tablet, film coatedGeneric drugs (ANDA)March 17, 2022
Lacosamide58118-8813Tablet, film coatedGeneric drugs (ANDA)March 17, 2022
Lacosamide58118-8812Tablet, film coatedGeneric drugs (ANDA)March 17, 2022
Gabapentin58118-1167TabletGeneric drugs (ANDA)October 1, 2021
Gabapentin58118-0166TabletGeneric drugs (ANDA)October 1, 2021

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.