Pleo Oku

Product NDC
60681-2402
11-digit product format
606812402
Labeler code
60681
Product ID
60681-2402_47621cb8-49dd-48fe-84a1-6be6402f2fc3
Type
HUMAN OTC DRUG
Nonproprietary name
OKOUBAKA AUBREVILLEI BARK
Dosage form
TABLET
Route
ORAL
Labeler
Sanum-Kehlbeck GmbH & Co. KG
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2012-07-10
Marketing end
0000-00-00
Substance
OKOUBAKA AUBREVILLEI BARK
Active strength
2 [hp_X]/1
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
60681-2402-22019-11-13C16284748780-197449f38-cd28-f6ea-e053-dbdaa90aa703Pleo ® Oku TABLETS 2X

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60681-2402-2Pleo Oku10 in 1 BLISTER PACKTABLET101
60681-2402-2Pleo Oku8 in 1 CARTONTABLET81

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60681-2402PLEO OKU (OKOUBAKA AUBREVILLEI BARK) TABLET [SANUM-KEHLBECK GMBH & CO. KG]1Legacy NDC, 2 package rows20120710_41bfd5b8-b123-4c14-a130-5bd27fd8692f.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
60681-2402-26068124020210 in 1 BLISTER PACKHistorical