Pulsatilla

Product NDC
57556-017
11-digit product format
575560017
Labeler code
57556
Product ID
57556-017_40941606-17ac-43f2-e063-6394a90acbc2
Type
HUMAN OTC DRUG
Nonproprietary name
Pulsatilla
Dosage form
PELLET
Route
ORAL
Labeler
Historical Remedies
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2021-07-06
Substance
ANEMONE PULSATILLA
Active strength
12 [hp_X]/g
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 PULSATILLA12 [hp_X]/g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiI76KB35JEV

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57556-017-02Pulsatilla14 g in 1 BOTTLE, GLASSPELLET149

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
57556-017PULSATILLA PELLET [HISTORICAL REMEDIES]8Current NDC, Legacy NDC, 1 package rows20241105_c6790a91-d601-8c37-e053-2995a90a0a0c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
57556-017-025755600170214 g in 1 BOTTLE, GLASS (57556-017-02) 14 g2021-07-060000-00-00NoNoCurrent