OKOUBAKA

Product NDC
59469-032
11-digit product format
594690032
Labeler code
59469
Product ID
59469-032_e3b50a80-d21e-4899-a4c4-50fea6d83bb2
Type
HUMAN OTC DRUG
Nonproprietary name
Okoubaka aubrevillei Bark
Dosage form
SOLUTION/ DROPS
Route
ORAL
Labeler
PEKANA Natuheilmittel GmbH
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2008-04-12
Substance
OKOUBAKA AUBREVILLEI BARK
Active strength
2 [hp_X]/50mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
OKOUBAKA
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
OKOUBAKA AUBREVILLEI BARK2 [hp_X]/50mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiMK2074187Z

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59469-032-10OKOUBAKA1 in 1 BOXSOLUTION/ DROPS15
59469-032-10OKOUBAKA50 mL in 1 BOTTLE, GLASSSOLUTION/ DROPS505

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59469-032OKOUBAKA (OKOUBAKA AUBREVILLEI BARK) SOLUTION/ DROPS [PEKANA NATUHEILMITTEL GMBH]5Current NDC, Legacy NDC, 2 package rows20221223_baeeb7ce-ab37-4a63-a825-66889a2df30f.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
59469-032-10594690032101 BOTTLE, GLASS in 1 BOX (59469-032-10) / 50 mL in 1 BOTTLE, GLASS2008-04-120000-00-00NoNoCurrent