FDA.reportPublic FDA data

Digitalis Purpurea

Product NDC
37662-0817
11-digit product format
376620817
Labeler code
37662
Product ID
37662-0817_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
12 [hp_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
Digitalis Purpurea
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
DIGITALIS12 [hp_C]/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiF1T8QT9U8B

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-0817-1Digitalis Purpurea200 in 1 VIAL, GLASSPELLET2001
37662-0817-2Digitalis Purpurea1200 in 1 BOTTLE, GLASSPELLET12001
37662-0817-3Digitalis Purpurea4000 in 1 BOTTLE, GLASSPELLET40001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-0817DIGITALIS PURPUREA PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, Legacy NDC, 3 package rows20220714_e3a004d3-f770-e4e9-e053-2995a90ab43c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
37662-0817-137662081701200 PELLET in 1 VIAL, GLASS (37662-0817-1) 200 pellet2022-07-120000-00-00NoNoCurrent
37662-0817-2376620817021200 PELLET in 1 BOTTLE, GLASS (37662-0817-2) 1200 pellet2022-07-120000-00-00NoNoCurrent
37662-0817-3376620817034000 PELLET in 1 BOTTLE, GLASS (37662-0817-3) 4000 pellet2022-07-120000-00-00NoNoCurrent