NDC11 00703321301

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
00703-3213-01	00703-3213
00703-3213-1	00703-3213
0703-3213-01	0703-3213

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
Paclitaxel	PACLITAXEL	Teva Parenteral Medicines, Inc.	e4be6cbf-72b9-4f7f-9b1b-459b2d35961a	2026-09-09	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 0703-3213-01 ndc (product): 0703-3213 ndc11 (package): 00703321301
Paclitaxel	PACLITAXEL	Teva Parenteral Medicines, Inc.	fbd32bd2-9685-41cb-bee2-730a45526b65	2026-07-11	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (product): 0703-3213

Reported adverse events (FAERS/openFDA)#

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