Kali bromatum

Product NDC
0220-2821
11-digit product format
002202821
Labeler code
0220
Product ID
0220-2821_0a0e1685-b647-7e21-e063-6394a90a5324
Type
HUMAN OTC DRUG
Nonproprietary name
POTASSIUM BROMIDE
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1983-03-03
Substance
POTASSIUM BROMIDE
Active strength
12 [hp_C]/12[hp_C]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Kali bromatum
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
POTASSIUM BROMIDE12 [hp_C]/12[hp_C]

Harmonized Identifiers#

Field, Values table
FieldValues
UniiOSD78555ZM

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-2821-412023-11-13C16284748780-1f386c649-d40c-0266-e053-dadaa90a7c1aKali bromatum 12C
0220-2821-412023-01-30C16284748780-1f386c649-d40c-0266-e053-dadaa90a7c1aKali bromatum 12C

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-2821-41Kali bromatum12 [hp_C] in 1 TUBEPELLET122

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-2821KALI BROMATUM (POTASSIUM BROMIDE ) PELLET [BOIRON]2Current NDC, Legacy NDC, 1 package rows20231114_8516c397-5f9c-2ac6-e053-2991aa0a9895.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-2821-410022028214112 [hp_C] in 1 TUBE (0220-2821-41) 1983-03-030000-00-00NoNoCurrent