Digitalis Purpurea

Product NDC
37662-0821
11-digit product format
376620821
Labeler code
37662
Product ID
37662-0821_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
500 [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
DIGITALIS500 [hp_C]/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiF1T8QT9U8B

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-0821-1Digitalis Purpurea200 in 1 VIAL, GLASSPELLET2001
37662-0821-2Digitalis Purpurea500 in 1 VIAL, GLASSPELLET5001
37662-0821-3Digitalis Purpurea3000 in 1 BOTTLE, GLASSPELLET30001
37662-0821-4Digitalis Purpurea10000 in 1 BOTTLE, GLASSPELLET100001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-0821DIGITALIS PURPUREA PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, Legacy NDC, 4 package rows20220714_e3a004d3-f770-e4e9-e053-2995a90ab43c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
37662-0821-137662082101200 PELLET in 1 VIAL, GLASS (37662-0821-1) 200 pellet2022-07-120000-00-00NoNoCurrent
37662-0821-237662082102500 PELLET in 1 VIAL, GLASS (37662-0821-2) 500 pellet2022-07-120000-00-00NoNoCurrent
37662-0821-3376620821033000 PELLET in 1 BOTTLE, GLASS (37662-0821-3) 3000 pellet2022-07-120000-00-00NoNoCurrent
37662-0821-43766208210410000 PELLET in 1 BOTTLE, GLASS (37662-0821-4) 10000 pellet2022-07-120000-00-00NoNoCurrent