Public directory / Facility profile
AR · FDA-registered outsourcing facility (503B). A factual public-record profile built from FDA sources, with dates. It is not a ranking, grade, or endorsement.
FDA 503B list ✓ (current 2026-07-14)
SCA Pharmaceuticals, Little Rock appears on FDA's registered outsourcing facilities list, parsed from Veritura's capture of that list (FDA list current as of 2026-07-14, captured 2026-07-17). Registration status can change between captures; the FDA page is the authoritative current source.
On FDA's list since we began tracking captures on 2026-07-11 (tracking began 2026-07-10; we make no claim about FDA's list before our first capture). Last confirmed on our 2026-07-17 capture (FDA list current as of 2026-07-14).
Dates are Veritura's own capture dates of FDA's public list, shown next to FDA's list-current date wherever we have it. Public-record posture, not a determination.
3 dated enforcement records matched this firm name in openFDA when this check last completed.
Source: openFDA enforcement records (drug/device/food, updated weekly), checked 2026-07-18. Dated public records matching this firm name; similar firm names collide in public records, so confirm the firm identity against the source records before relying. Public-record posture, not a determination.
3 enforcement record matches on this firm name in openFDA when this screen last ran. Review the underlying public records and confirm the firm identity before relying on this signal.
0 FDA compliance action records matched this name.
Source: openFDA enforcement records and FDA compliance dashboards, refreshed at most every 6 hours. A count here documents what public sources returned for this name (searched: SCA Pharmaceuticals, Little Rock); it is not a Veritura determination about the facility.
No product reports matched this facility name in our FDA data (reporting periods queried: 2025-2, 2025-1). Product reports are matched on the establishment name FDA prints, which can differ from the roster name; absence here is a name-match result, not a statement that the facility reported nothing.
Source: FDA outsourcing facility product reports (FD&C 503B(b)(2)), reported to FDA twice a year. Public-record posture, not a determination.
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Documented public status from FDA sources. Not an approval, ranking, or endorsement. Veritura does not rank facilities. Dates below show when FDA's list was current and when we captured it, not a Veritura verification of any facility.