FDA.reportPublic FDA data

NDC 0149-0734-02 - Dantrium

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
0149-0734
Requested NDC
0149-0734-02
Package NDCs from labels
0149-0734-02
Manufacturer
Procter and Gamble Pharmaceuticals
Effective date
2006-02-06
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Dantrium - Procter and Gamble PharmaceuticalsProcter and Gamble Pharmaceuticals2006-02-06HUMAN PRESCRIPTION DRUG LABELING

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
dantrolene sodiumACTIVE INGREDIENT287M0347EVDANTRIUM (DANTROLENE SODIUM) INJECTION [PROCTER AND GAMBLE PHARMACEUTICALS]2
dantroleneACTIVE MOIETYF64QU97QCRDANTRIUM (DANTROLENE SODIUM) INJECTION [PROCTER AND GAMBLE PHARMACEUTICALS]2
mannitolINACTIVE INGREDIENT3OWL53L36ADANTRIUM (DANTROLENE SODIUM) INJECTION [PROCTER AND GAMBLE PHARMACEUTICALS]2
sodium hydroxideINACTIVE INGREDIENT55X04QC32IDANTRIUM (DANTROLENE SODIUM) INJECTION [PROCTER AND GAMBLE PHARMACEUTICALS]2

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 ยท 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
AD57FBC5-DC8E-439B-9E56-099DF3B246B0ef4d3d9f-4976-4eae-92b1-77749de3c63c2006-02-06Warnings, Adverse reactionsExact identifier
spl id: AD57FBC5-DC8E-439B-9E56-099DF3B246B0
spl set id: ef4d3d9f-4976-4eae-92b1-77749de3c63c

Reported adverse events (FAERS/openFDA)#

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