NDC11 00121203630

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
00121-2036-30	00121-2036
0121-2036-30	0121-2036

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
Buprenorphine and Naloxone	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	PAI Holdings, LLC dba PAI Pharma	d5b011ef-f1be-47f2-8f8b-07553f36193c	2026-02-28	Warnings, Adverse reactions	Exact identifier ndc (package): 0121-2036-30 ndc (product): 0121-2036 ndc11 (package): 00121203630

Reported adverse events (FAERS/openFDA)#

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