Toxoplasma Gondii Homochord

Product NDC
43742-1133
11-digit product format
437421133
Labeler code
43742
Product ID
43742-1133_82bcbc32-6ae9-4667-8875-37fba1e71ea3
Type
HUMAN OTC DRUG
Nonproprietary name
Toxoplasma Gondii
Dosage form
LIQUID
Route
ORAL
Labeler
Deseret Biologicals, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2017-12-29
Marketing end
2025-02-28
Substance
TOXOPLASMA GONDII
Active strength
15 [hp_X]/mL
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43742-1133-14374211330130 mL in 1 BOTTLE, DROPPER (43742-1133-1) 30 ml2017-12-292025-02-28NoNoCurrent