Pleo Usti - 60681-5604-1 - (ustilago maydis)

Alphabetical Index


Drug Information of Pleo Usti

Product NDC: 60681-5604
Proprietary Name: Pleo Usti
Non Proprietary Name: ustilago maydis
Active Ingredient(s): 5    [HP_X]/1 & nbsp;   ustilago maydis
Administration Route(s): RECTAL
Dosage Form(s): SUPPOSITORY
Coding System: National Drug Codes(NDC)

Labeler Information of Pleo Usti

Product NDC: 60681-5604
Labeler Name: Sanum Kehlbeck GmbH & Co. KG
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20040421

Package Information of Pleo Usti

Package NDC: 60681-5604-1
Package Description: 1 DOSE PACK in 1 CARTON (60681-5604-1) > 10 SUPPOSITORY in 1 DOSE PACK

NDC Information of Pleo Usti

NDC Code 60681-5604-1
Proprietary Name Pleo Usti
Package Description 1 DOSE PACK in 1 CARTON (60681-5604-1) > 10 SUPPOSITORY in 1 DOSE PACK
Product NDC 60681-5604
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ustilago maydis
Dosage Form Name SUPPOSITORY
Route Name RECTAL
Start Marketing Date 20040421
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Sanum Kehlbeck GmbH & Co. KG
Substance Name USTILAGO MAYDIS
Strength Number 5
Strength Unit [HP_X]/1
Pharmaceutical Classes

Complete Information of Pleo Usti


General Information