Pulsatilla

Product NDC
0220-4184
11-digit product format
002204184
Labeler code
0220
Product ID
0220-4184_f187d890-3908-8614-e053-2a95a90ab91d
Type
HUMAN OTC DRUG
Nonproprietary name
ANEMONE PULSATILLA
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1983-03-03
Substance
ANEMONE PULSATILLA
Active strength
15 [hp_C]/15[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
Pulsatilla
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ANEMONE PULSATILLA15 [hp_C]/15[hp_C]

Harmonized Identifiers#

Field, Values table
FieldValues
UniiI76KB35JEV

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-4184-41Pulsatilla15 [hp_C] in 1 TUBEPELLET152

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-4184PULSATILLA (ANEMONE PULSATILLA ) PELLET [BOIRON]2Current NDC, Legacy NDC, 1 package rows20230106_86a84380-94f4-41f2-e053-2991aa0a870b.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-4184-410022041844115 [hp_C] in 1 TUBE (0220-4184-41) 1983-03-030000-00-00NoNoCurrent