Pulsatilla

Product NDC
76472-3030
11-digit product format
764723030
Labeler code
76472
Product ID
76472-3030_2ddc5fae-8d3c-7121-e063-6294a90a6aad
Type
HUMAN OTC DRUG
Nonproprietary name
Pulsatilla
Dosage form
PELLET
Route
SUBLINGUAL
Labeler
SEVENE USA
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2011-11-23
Substance
PULSATILLA ALPINA WHOLE
Active strength
200 [kp_C]/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Pulsatilla
Brand name suffix
200ck
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
PULSATILLA ALPINA WHOLE200 [kp_C]/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii6J43Y8MXF0

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76472-3030-1Pulsatilla200ck80 in 1 CYLINDERPELLET804

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76472-3030PULSATILLA 200CK (PULSATILLA) PELLET [SEVENE USA]4Current NDC, Legacy NDC, 1 package rows20250213_cf8960de-0eee-728e-e053-2a95a90a67ce.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
76472-3030-17647230300180 PELLET in 1 CYLINDER (76472-3030-1) 80 pellet2011-11-230000-00-00NoNoCurrent