NDC11 68788713004

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
68788-7130-04	68788-7130
68788-7130-4	68788-7130

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
ALENDRONATE SODIUM	ALENDRONATE SODIUM	Preferred Pharmaceuticals Inc.	83e3ba94-d882-4b5c-87cb-af1eb0997efc	2026-02-16	Warnings, Adverse reactions	Exact identifier ndc (package): 68788-7130-4 ndc (product): 68788-7130 ndc11 (package): 68788713004

Reported adverse events (FAERS/openFDA)#

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