NDC11 68071165005

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
68071-1650-05	68071-1650
68071-1650-5	68071-1650

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
Sulfacetamide Sodium and Prednisolone Sodium Phosphate	SULFACETAMIDE SODIUM AND PREDNISOLONE SODIUM PHOSPHATE	NuCare Pharmaceuticals,Inc.	835def0b-ed5a-61a0-e053-2a91aa0ae7ae	2024-07-15	Warnings, Adverse reactions	Exact identifier ndc (package): 68071-1650-5 ndc (product): 68071-1650 ndc11 (package): 68071165005

Reported adverse events (FAERS/openFDA)#

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