NDC11 43386070083

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
43386-0700-83	43386-0700
43386-700-83	43386-700

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
SODIUM SULFATE, POTASSIUM SULFATE, MAGNESIUM SULFATE	SODIUM SULFATE, POTASSIUM SULFATE, MAGNESIUM SULFATE	Lupin Pharmaceuticals, Inc.	d4883657-d27d-4056-a567-5fb12d5e05d1	2025-12-15	Warnings, Adverse reactions	Exact identifier ndc (package): 43386-700-83 ndc (product): 43386-700 ndc11 (package): 43386070083

Reported adverse events (FAERS/openFDA)#

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