Pleo Usti

Product NDC
60681-5603
11-digit product format
606815603
Labeler code
60681
Product ID
60681-5603_c44bf99d-7fef-477e-abf2-7d79fd15e2d5
Type
HUMAN OTC DRUG
Nonproprietary name
ustilago maydis
Dosage form
SOLUTION/ DROPS
Route
ORAL
Labeler
Sanum Kehlbeck GmbH & Co. KG
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1998-01-19
Marketing end
0000-00-00
Substance
USTILAGO MAYDIS
Active strength
5 [HP_X]/10mL
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60681-5603-12019-10-21C16284748780-1956f9ecf-c77d-621f-e053-dbdaa90a74adPleo™ Usti PORTABLE SIPS 5X
60681-5603-22019-10-21C16284748780-1956f9ecf-c77d-621f-e053-dbdaa90a74adPleo™ Usti PORTABLE SIPS 5X

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60681-5603-1Pleo Usti1 mL in 1 VIAL, GLASSSOLUTION/ DROPS11
60681-5603-1Pleo Usti10 in 1 CARTONSOLUTION/ DROPS101
60681-5603-2Pleo Usti1 mL in 1 VIAL, GLASSSOLUTION/ DROPS11
60681-5603-2Pleo Usti50 in 1 CARTONSOLUTION/ DROPS501

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60681-5603PLEO USTI (USTILAGO MAYDIS) SOLUTION/ DROPS [SANUM KEHLBECK GMBH & CO. KG]1Legacy NDC, 4 package rows20110113_41c3d8a9-c80e-4d1b-a954-38d678877cd3.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
60681-5603-1606815603011 mL in 1 VIAL, GLASS1 mlHistorical
60681-5603-2606815603021 mL in 1 VIAL, GLASS1 mlHistorical