The current product page lists multiple injectable Semaglutide Flex-Dose strengths and volumes.
Tirzepatide
The current product page lists multiple injectable Tirzepatide Flex-Dose strengths and volumes.
Product-page presence does not establish availability in every state or for every patient.
Locations in the source record
2666 SW 36th St, Fort Lauderdale, FL 33312
Services named by sources
Patient-specific compounded medications
Sterile compounding
Injectable compounded products
Practitioner and patient fulfillment
Regulatory compliance
503 pathway evidence
A pathway label describes which federal rules apply — it is not a quality claim.
Section 503A
Source-backed pathway evidence
Hallandale describes itself as a 503A pharmacy. FDA's compounding-action index also labels the facility type 503A. Section 503A is a statutory compounding pathway, not an FDA facility registration.
Section 503B
Not conclusively established
No exact Hallandale/Pharmcore match was found in the FDA current registered-outsourcing-facility list checked on 2026-08-20. This is recorded as a bounded registry result, not a categorical claim that no affiliated 503B entity exists.
Telehealth providers
No provider relationship is verified in the bound sources.
Clinic Scout links a provider only when an explicit source names the relationship.
FDA warning-letter, Form 483, compounding-action, current 503B-registry, and Florida license sources were checked. Florida's accessible license record showed no discipline on file in the agent result; other state-board action searches were not exhaustively completed.
U.S. Food and Drug Administration · 2020-03-11
Warning Letter
FDA stated that investigators observed serious deficiencies in sterile-drug production, insanitary conditions, and drug products that did not meet all conditions of section 503A. FDA later stated that Pharmcore appeared to have adequately addressed the violations in this warning letter.
closed_out_2022-05-03
U.S. Food and Drug Administration · 2025-06-13
Form FDA 483
FDA listed three inspection observations concerning calibration response, complaint review/procedures, and stability/reprocessing support. A Form 483 records inspection observations and is not itself a final agency determination.
issued
What remains unverified
Full state-by-state license and shipping footprint
During the inspection, the FDA investigators observed serious deficiencies in your practices for producing drug products intended or expected to be sterile, which put patients at risk.
Updated as of 8/18/2026 ... This table lists the outsourcing facilities that have submitted registration information that has been determined to be complete by the data lock date for the latest weekly update of the table.
Related evidence records
Continue with records sharing source-backed directory tags.
These links are based only on shared GLP-1 relevance or 503-pathway tags; they do not assert affiliation or a dispensing relationship.
GLP Clinic Scout does not issue a blanket legitimacy verdict. This research record preserves 8 dated first-party or regulator citation(s), 2 regulatory/action record(s), and 3 explicitly unresolved field(s). Review the cited evidence and current license status before making a decision.
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