Fraxinus americana

Product NDC
0220-2156
11-digit product format
002202156
Labeler code
0220
Product ID
0220-2156_f52926bd-b7fb-8070-e053-2a95a90ac58d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
FRAXINUS AMERICANA BARK
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1983-03-03
Substance
FRAXINUS AMERICANA BARK
Active strength
30 [hp_C]/30[hp_C]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
FRAXINUS AMERICANA BARK30 [hp_C]/30[hp_C]

Harmonized Identifiers#

Field, Values table
FieldValues
Unii0B24UR1O1S

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-2156-412023-02-20C16284748780-1f386c64a-2b4c-0266-e053-dadaa90a7c1aFraxinus americana 30C
0220-2156-412023-01-30C16284748780-1f386c64a-2b4c-0266-e053-dadaa90a7c1aFraxinus americana 30C

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-2156-41Fraxinus americana30 [hp_C] in 1 TUBEPELLET302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-2156FRAXINUS AMERICANA (FRAXINUS AMERICANA BARK ) PELLET [BOIRON]2Current NDC, Legacy NDC, 1 package rows20230222_85a180d8-01c6-78b8-e053-2991aa0aed90.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-2156-410022021564130 [hp_C] in 1 TUBE (0220-2156-41) 1983-03-030000-00-00NoNoCurrent