Pleo Usti - 60681-5603-1 - (ustilago maydis)

Alphabetical Index


Drug Information of Pleo Usti

Product NDC: 60681-5603
Proprietary Name: Pleo Usti
Non Proprietary Name: ustilago maydis
Active Ingredient(s): 5    [HP_X]/10mL & nbsp;   ustilago maydis
Administration Route(s): ORAL
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Pleo Usti

Product NDC: 60681-5603
Labeler Name: Sanum Kehlbeck GmbH & Co. KG
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 19980119

Package Information of Pleo Usti

Package NDC: 60681-5603-1
Package Description: 10 VIAL, GLASS in 1 CARTON (60681-5603-1) > 1 mL in 1 VIAL, GLASS

NDC Information of Pleo Usti

NDC Code 60681-5603-1
Proprietary Name Pleo Usti
Package Description 10 VIAL, GLASS in 1 CARTON (60681-5603-1) > 1 mL in 1 VIAL, GLASS
Product NDC 60681-5603
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ustilago maydis
Dosage Form Name SOLUTION/ DROPS
Route Name ORAL
Start Marketing Date 19980119
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Sanum Kehlbeck GmbH & Co. KG
Substance Name USTILAGO MAYDIS
Strength Number 5
Strength Unit [HP_X]/10mL
Pharmaceutical Classes

Complete Information of Pleo Usti


General Information