NDC11 64208251204

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
64208-2512-04	64208-2512
64208-2512-4	64208-2512

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 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
BEIZRAY	DOCETAXEL	Zydus Pharmaceuticals USA Inc.	8fb7d980-d6c7-468b-a9f0-adff16101a4b	2025-12-17	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 64208-2512-4 ndc11 (package): 64208251204
ALBUMINEX	ALBUMIN HUMAN	BPL	167f48d0-8ae5-4f7e-b050-9673dad78acc	2024-12-31	Warnings, Adverse reactions	Exact identifier ndc (package): 64208-2512-4 ndc (product): 64208-2512 ndc11 (package): 64208251204

Reported adverse events (FAERS/openFDA)#

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