NDC11 00641603901

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
00641-6039-01	00641-6039
00641-6039-1	00641-6039
0641-6039-01	0641-6039

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
INFUMORPH 200	MORPHINE SULFATE	Hikma Pharmaceuticals USA Inc.	db9ac9e3-d761-4a99-9f34-4946ebe8f255	2025-12-31	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 0641-6039-01 ndc (product): 0641-6039 ndc11 (package): 00641603901

Reported adverse events (FAERS/openFDA)#

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