Pleo Oku

Product NDC
60681-2401
11-digit product format
606812401
Labeler code
60681
Product ID
60681-2401_1bdccfcb-ad36-4760-a746-c699b708a215
Type
HUMAN OTC DRUG
Nonproprietary name
OKOUBAKA AUBREVILLEI BARK
Dosage form
SOLUTION/ DROPS
Route
ORAL
Labeler
Sanum Kehlbeck GmbH & Co. KG
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1996-03-19
Marketing end
0000-00-00
Substance
OKOUBAKA AUBREVILLEI BARK
Active strength
2 [hp_X]/30mL
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
60681-2401-32019-10-21C16284748780-1956f9ecf-d20c-621f-e053-dbdaa90a74adPleo™ Oku DROPS 2X

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60681-2401-3Pleo Oku1 in 1 CARTONSOLUTION/ DROPS12
60681-2401-3Pleo Oku30 mL in 1 BOTTLE, DROPPERSOLUTION/ DROPS302

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60681-2401PLEO OKU (OKOUBAKA AUBREVILLEI BARK) SOLUTION/ DROPS [SANUM KEHLBECK GMBH & CO. KG]2Legacy NDC, 2 package rows20110114_4d1c63f3-ceb5-42b2-a71e-0659a46ca8eb.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
60681-2401-3606812401031 in 1 CARTONHistorical