Quercetin - 43742-0217-1 - (Quercetin)

Alphabetical Index


Drug Information of Quercetin

Product NDC: 43742-0217
Proprietary Name: Quercetin
Non Proprietary Name: Quercetin
Active Ingredient(s): 6    [hp_X]/mL & nbsp;   Quercetin
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Quercetin

Product NDC: 43742-0217
Labeler Name: Deseret Biologicals, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20130411

Package Information of Quercetin

Package NDC: 43742-0217-1
Package Description: 30 mL in 1 BOTTLE, DROPPER (43742-0217-1)

NDC Information of Quercetin

NDC Code 43742-0217-1
Proprietary Name Quercetin
Package Description 30 mL in 1 BOTTLE, DROPPER (43742-0217-1)
Product NDC 43742-0217
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Quercetin
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20130411
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Deseret Biologicals, Inc.
Substance Name QUERCETIN
Strength Number 6
Strength Unit [hp_X]/mL
Pharmaceutical Classes

Complete Information of Quercetin


General Information