NDC11 43742169801

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
43742-1698-01	43742-1698
43742-1698-1	43742-1698

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
BACT COMBINATION	ADENOSINUM TRIPHOSPHORICUM DINATRUM, MALICUM ACIDUM, NATRUM OXALACETICUM, OROTICUM ACIDUM, RIBOFLAVINUM, CINNAMIC ACID, PETROSELINUM SATIVUM, COLIBACILLINUM CUM NATRUM MURIATICUM, ECHINACEA (ANGUSTIFOLIA), HELICOBACTER PYLORI, MYCOPLASMA PNEUMONIAE, PROTEUS (MIRABILIS), PROTEUS (VULGARIS), PSEUDOMONAS AERUGINOSA, SALMONELLA TYPHI NOSODE, ENTEROCOCCUS FAECALIS, STREPTOCOCCUS MUTANS, PNEUMOCOCCINUM, STREPTOCOCCUS AGALACTIAE, LEGIONELLA PNEUMOPHILA, LISTERIA MONOCYTOGENES, DYSENTERY BACILLUS, SHIGELLA SONNEI,	Deseret Biologicals, Inc.	e11b176e-7958-4d5b-b5ad-a1174f23ecf3	2024-02-06	Warnings	Exact identifier ndc (package): 43742-1698-1 ndc (product): 43742-1698 ndc11 (package): 43742169801

Reported adverse events (FAERS/openFDA)#

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