NDC11 70518012204

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
70518-0122-04	70518-0122
70518-0122-4	70518-0122
70518-122-04	70518-122

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
Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	REMEDYREPACK INC.	b9f20917-9529-4c62-bafe-baae7f8d6c77	2026-06-23	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 70518-0122-4 ndc (product): 70518-0122 ndc11 (package): 70518012204

Reported adverse events (FAERS/openFDA)#

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