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APS Pharmacy (Drug Depot, LLC)

Clearwater, FL·503A
Past issue, resolved·Last checked August 17, 2026.

Past issue, resolved — closeout on file (Oct 2023).

About this pharmacy

Legal entity: Drug Depot, LLC dbai APS Pharmacy
Facility type: 503A compounding pharmacyi.

The four standards

01
Accredited— Not yet evaluated

This standard has not yet been checked for this pharmacy.

02
Regulatory record— Past issue, resolved

In 2023, FDA inspectors found that drug products produced at this facility did not qualify for 503Ai compounding exemptions and that bulk drug substances were sourced from establishments not registered with FDA. APS Pharmacy corrected it, and FDA formally confirmed the correction in 2023.

(Method: checked against FDA’s public warning-letter and closeout-letter databases.)

Source: FDA warning letter — March 2023

Source: FDA closeout letter — October 2023

03
Openly named— Not yet evaluated

This standard has not yet been checked for this pharmacy.

04
Shipping reputation— Not yet evaluated

This standard has not yet been checked for this pharmacy.

Notes

Context
Note on Belmar relationship— Not independently confirmed

This entity’s warning and closeout letters list Belmar Pharma Solutions leadership as CC’d contacts, suggesting a possible corporate/quality-oversight relationship. This relationship is not independently confirmed, so APS Pharmacy’s record is reported on its own rather than attributed to Belmar.

Frequently asked questions

Is APS Pharmacy (Drug Depot, LLC) accredited?

Accreditation has not yet been evaluated for APS Pharmacy (Drug Depot, LLC). This standard has not yet been checked for this pharmacy, so we cannot confirm or deny accreditation status at this time.

Has APS Pharmacy (Drug Depot, LLC) had any FDA regulatory actions?

Yes, but it was resolved. In 2023, FDA inspectors found that drug products produced at this facility did not qualify for 503A compounding exemptions and that bulk drug substances were sourced from establishments not registered with FDA. APS Pharmacy corrected it, and FDA formally confirmed the correction in 2023. Checked against FDA’s public warning-letter and closeout-letter databases.

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