NDC11 62756052940

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
62756-0529-40	62756-0529
62756-529-40	62756-529

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
Desmopressin Acetate	DESMOPRESSIN ACETATE	Sun Pharmaceutical Industries, Inc.	9fd48eec-aa24-4888-b99f-d409ada958a7	2022-08-24	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 62756-529-40 ndc (product): 62756-529 ndc11 (package): 62756052940
desmopressin acetate	DESMOPRESSIN ACETATE	Sun Pharmaceutical Industries, Inc.	2dc2cec8-6953-4a33-9356-11534fba1fb8	2020-01-23	Warnings, Adverse reactions	Exact identifier ndc (product): 62756-529

Reported adverse events (FAERS/openFDA)#

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