"69597-921-01" National Drug Code (NDC)

NDC Code	69597-921-01
Package Description	100 g in 1 CONTAINER (69597-921-01)
Product NDC	69597-921
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Xizflus
Non-Proprietary Name	Sodium Polysulthionate And 5-methyltetrahydrofolate
Dosage Form	POWDER
Usage	ORAL; TOPICAL
Start Marketing Date	20150714
End Marketing Date	20300101
Marketing Category Name	UNAPPROVED DRUG OTHER
Manufacturer	Basiem
Substance Name	SULFUR; SODIUM SULFATE; SODIUM THIOSULFATE; LEVOMEFOLIC ACID
Strength	97; 2; .45; .125
Strength Unit	g/100g; g/100g; g/100g; g/100g