NDC11 00574082001

This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.

Possible FDA NDC forms#

Package NDC, Product root table
Package NDCProduct root
00574-0820-0100574-0820
00574-0820-100574-0820
00574-820-0100574-820
0574-0820-010574-0820

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 ยท 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Testone CIKTESTOSTERONE CYPIONATE, ALCOHOLAsclemed USA, Inc.edcd5209-70db-4727-991e-3fdd185d92112026-01-11Warnings, Adverse reactionsExact identifier
ndc (package): 0574-0820-01
ndc11 (package): 00574082001
Testosterone CypionateTESTOSTERONE CYPIONATEPadagis US LLC4195516a-c8e6-457c-b805-43c9a3ca8b772025-06-03Warnings, Adverse reactionsExact identifier
ndc (package): 0574-0820-01
ndc (product): 0574-0820
ndc11 (package): 00574082001

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.