FDA.reportPublic FDA data

Melilotus Alba

Product NDC
37662-2496
11-digit product format
376622496
Labeler code
37662
Product ID
37662-2496_f31d91d4-3254-7100-e053-2995a90a10f2
Type
HUMAN OTC DRUG
Nonproprietary name
Melilotus Alba
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2023-01-25
Substance
MELILOTUS ALBUS TOP
Active strength
100 [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
Melilotus Alba
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MELILOTUS ALBUS TOP100 [hp_C]/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii123T84GFBH

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-2496-1Melilotus Alba200 in 1 VIAL, GLASSPELLET2001
37662-2496-2Melilotus Alba500 in 1 VIAL, GLASSPELLET5001
37662-2496-3Melilotus Alba3000 in 1 BOTTLE, GLASSPELLET30001
37662-2496-4Melilotus Alba10000 in 1 BOTTLE, GLASSPELLET100001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-2496MELILOTUS ALBA PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, 4 package rows20230127_f31d91d4-3253-7100-e053-2995a90a10f2.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
37662-2496-137662249601200 PELLET in 1 VIAL, GLASS (37662-2496-1) 200 pellet2023-01-25NoNoCurrent
37662-2496-237662249602500 PELLET in 1 VIAL, GLASS (37662-2496-2) 500 pellet2023-01-25NoNoCurrent
37662-2496-3376622496033000 PELLET in 1 BOTTLE, GLASS (37662-2496-3) 3000 pellet2023-01-25NoNoCurrent
37662-2496-43766224960410000 PELLET in 1 BOTTLE, GLASS (37662-2496-4) 10000 pellet2023-01-25NoNoCurrent