NDC11 00517079101

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
00517-0791-01	00517-0791
00517-0791-1	00517-0791
00517-791-01	00517-791
0517-0791-01	0517-0791

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
Betamethasone Sodium Phosphate and Betamethasone Acetate	BETAMETHASONE SODIUM PHOSPHATE AND BETAMETHASONE ACETATE	American Regent, Inc.	335f17e7-069d-456c-8507-26253692f2ee	2025-11-19	Warnings, Adverse reactions	Exact identifier ndc (package): 0517-0791-01 ndc (product): 0517-0791 ndc11 (package): 00517079101

Reported adverse events (FAERS/openFDA)#

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