NDC11 00121097450

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 NDC	Product root
00121-0974-50	00121-0974
00121-974-50	00121-974
0121-0974-50	0121-0974

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 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Sucralfate	SUCRALFATE	PAI Holdings, LLC dba PAI Pharma	113a068a-2ce9-421c-8b89-87ce30e19225	2026-03-11	Warnings, Adverse reactions	Exact identifier ndc (package): 0121-0974-50 ndc (product): 0121-0974 ndc11 (package): 00121097450

Reported adverse events (FAERS/openFDA)#

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