NDC11 64380011602

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
64380-0116-02	64380-0116
64380-0116-2	64380-0116
64380-116-02	64380-116

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 and Magnesium Sulfate Oral	SODIUM SULFATE, POTASSIUM SULFATE AND MAGNESIUM SULFATE ORAL	Strides Pharma Science Limited	d48d8c59-68b9-4e28-86a4-eabf8b2003b0	2026-03-10	Warnings, Adverse reactions	Exact identifier ndc (package): 64380-116-02 ndc (product): 64380-116 ndc11 (package): 64380011602

Reported adverse events (FAERS/openFDA)#

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