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FDA compounder NDC directory

Browse every current FDA compounder source row, including records that do not contain a usable NDC.

Compounder NDC directory#

Every current compounder source row is browsable, including records whose FDA source did not provide a usable product, package, or lookup NDC. Browse the unified current auxiliary catalog. · Browse the complete captured source and snapshot history.

Compounder directory page 1 of 1 · 5 matching rows.

Establishment, FEI, Product NDC table
EstablishmentFEIProduct NDCPackage NDCBrandNonproprietary nameActive ingredientsPeriodNormalizationSource date
Hybrid Pharma07966574226436-517726436-5177-2Alprostadil; Papaverine Hydrobromide; Phentolamine Mesylate50 ug/1 mL; 30 mg/1 mL; 2 mg/1 mL2025-1valid2026-10-13
Hybrid Pharma26436-517726436-5177-2Trimix 50/30/2Trimix 50/30/250 ug/1 mL; 30 mg/1 mL; 2 mg/1 mL2025-1valid2026-09-18
Hybrid Pharma07966574226436-517726436-5177-2Alprostadil; Papaverine Hydrobromide; Phentolamine Mesylate50 ug/1 mL; 30 mg/1 mL; 2 mg/1 mL2024-1valid2026-10-13
Hybrid Pharma07966574226436-517726436-5177-2Alprostadil; Papaverine Hydrobromide; Phentolamine Mesylate50 ug/1 mL; 30 mg/1 mL; 2 mg/1 mL2023-2valid2026-10-13
Hybrid Pharma07966574226436-517726436-5177-2Papaverine Hydrobromide; Phentolamine Mesylate; Alprostadil30 mg/1 mL; 2 mg/1 mL; 50 ug/1 mL2021-2valid2026-10-13