NDC11 00069013501

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
00069-0135-01	00069-0135
00069-0135-1	00069-0135
00069-135-01	00069-135
0069-0135-01	0069-0135

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
BOSULIF	BOSUTINIB	Pfizer Laboratories Div Pfizer Inc	adc84ad5-a04d-4fee-9ba8-91f7abd928e3	2026-03-10	Warnings, Adverse reactions	Exact identifier ndc (package): 0069-0135-01 ndc (product): 0069-0135 ndc11 (package): 00069013501

Reported adverse events (FAERS/openFDA)#

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