Digitalis Purpurea

Product NDC
37662-0824
11-digit product format
376620824
Labeler code
37662
Product ID
37662-0824_e3a004d3-f771-e4e9-e053-2995a90ab43c
Type
HUMAN OTC DRUG
Nonproprietary name
Digitalis Purpurea
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2022-07-12
Substance
DIGITALIS
Active strength
1 [hp_Q]/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Digitalis Purpurea
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
DIGITALIS1 [hp_Q]/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiF1T8QT9U8B

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-0824-1Digitalis Purpurea10000 in 1 BOTTLE, GLASSPELLET100001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-0824DIGITALIS PURPUREA PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, Legacy NDC, 1 package rows20220714_e3a004d3-f770-e4e9-e053-2995a90ab43c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
37662-0824-13766208240110000 PELLET in 1 BOTTLE, GLASS (37662-0824-1) 10000 pellet2022-07-120000-00-00NoNoCurrent