NDC11 43742141401

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
43742-1414-01	43742-1414
43742-1414-1	43742-1414

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
BP Reg	ALLIUM SATIVUM, ADRENALINUM, ARTERIA SUIS, CORTISONE ACETICUM, THYROIDINUM (SUIS), VENA SUIS, FORMALINUM, KALI CHLORICUM, ALPHA-LIPOICUM ACIDUM, AURUM METALLICUM, CACTUS GRANDIFLORUS, CHOLESTERINUM, COUMARINUM, EPHEDRA VULGARIS, GLONOINUM, LACHESIS MUTUS, RAUWOLFIA SERPENTINA, STRONTIUM CARBONICUM, SULPHUR, VERATRUM ALBUM, PROTEUS (VULGARIS)	Deseret Biologicals, Inc.	f99833d8-d637-4c63-afe8-25eb2f05de6a	2024-05-08	Warnings	Exact identifier ndc (package): 43742-1414-1 ndc (product): 43742-1414 ndc11 (package): 43742141401

Reported adverse events (FAERS/openFDA)#

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