NDC11 81033012344

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
81033-0123-44	81033-0123
81033-123-44	81033-123

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 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Gabapentin	GABAPENTIN	Kesin Pharma Corporation	4470a567-93a6-a293-e063-6394a90affc1	2025-11-25	Warnings, Adverse reactions	Exact identifier ndc (product): 81033-123
Gabapentin	GABAPENTIN	Kesin Pharma Corporation	3f2ba3d6-6086-eaf2-e063-6294a90a7642	2025-09-19	Warnings, Adverse reactions	Exact identifier ndc (package): 81033-123-44 ndc (product): 81033-123 ndc11 (package): 81033012344

Reported adverse events (FAERS/openFDA)#

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