FDA.reportPublic FDA data

Pulsatilla Nigricans

Product NDC
37662-4021
11-digit product format
376624021
Labeler code
37662
Product ID
37662-4021_063800f4-7ae8-0e3f-e063-6294a90a537a
Type
HUMAN OTC DRUG
Nonproprietary name
Pulsatilla Nigricans
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2023-09-25
Substance
PULSATILLA PRATENSIS WHOLE
Active strength
1 [hp_M]/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 Nigricans
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
PULSATILLA PRATENSIS WHOLE1 [hp_M]/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii8E272251DI

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-4021-1Pulsatilla Nigricans200 in 1 VIAL, GLASSPELLET2001
37662-4021-2Pulsatilla Nigricans500 in 1 VIAL, GLASSPELLET5001
37662-4021-3Pulsatilla Nigricans3000 in 1 BOTTLE, GLASSPELLET30001
37662-4021-4Pulsatilla Nigricans10000 in 1 BOTTLE, GLASSPELLET100001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-4021PULSATILLA NIGRICANS PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, 4 package rows20230926_063800f4-7ae7-0e3f-e063-6294a90a537a.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
37662-4021-137662402101200 PELLET in 1 VIAL, GLASS (37662-4021-1) 200 pellet2023-09-25NoNoHistorical
37662-4021-237662402102500 PELLET in 1 VIAL, GLASS (37662-4021-2) 500 pellet2023-09-25NoNoHistorical
37662-4021-3376624021033000 PELLET in 1 BOTTLE, GLASS (37662-4021-3) 3000 pellet2023-09-25NoNoHistorical
37662-4021-43766240210410000 PELLET in 1 BOTTLE, GLASS (37662-4021-4) 10000 pellet2023-09-25NoNoHistorical