NDC11 00121107004

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
00121-1070-04	00121-1070
00121-1070-4	00121-1070
0121-1070-04	0121-1070

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
Promethazine DM	PROMETHAZINE HYDROCHLORIDE AND DEXTROMETHORPHAN HYDROBROMIDE	PAI Holdings, LLC dba PAI Pharma	1d47280d-28c9-4701-8c5f-a6e6b524083b	2025-05-31	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 0121-1070-04 ndc (product): 0121-1070 ndc11 (package): 00121107004

Reported adverse events (FAERS/openFDA)#

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