kali bromatum
Generic: potassium bromide
Labeler: boironDrug Facts
Product Profile
Brand Name
kali bromatum
Generic Name
potassium bromide
Labeler
boiron
Dosage Form
PELLET
Routes
Active Ingredients
potassium bromide 9 [hp_C]/9[hp_C]
Manufacturer
Identifiers & Regulatory
Product NDC
0220-2820
Product ID
0220-2820_0a0e1efd-9eb4-83d7-e063-6294a90a9643
Product Type
HUMAN OTC DRUG
Marketing Category
UNAPPROVED HOMEOPATHIC
Listing Expiration
2026-12-31
Marketing Start
1983-03-03
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
02202820
Hyphenated Format
0220-2820
Supplemental Identifiers
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
kali bromatum (source: ndc)
Generic Name
potassium bromide (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 9 [hp_C]/9[hp_C]
Packaging
- 9 [hp_C] in 1 TUBE (0220-2820-41)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0a0e1efd-9eb4-83d7-e063-6294a90a9643", "openfda": {"unii": ["OSD78555ZM"], "spl_set_id": ["8516abc2-fc68-30ac-e053-2a91aa0ae0d6"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "9 [hp_C] in 1 TUBE (0220-2820-41)", "package_ndc": "0220-2820-41", "marketing_start_date": "19830303"}], "brand_name": "Kali bromatum", "product_id": "0220-2820_0a0e1efd-9eb4-83d7-e063-6294a90a9643", "dosage_form": "PELLET", "product_ndc": "0220-2820", "generic_name": "POTASSIUM BROMIDE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Kali bromatum", "active_ingredients": [{"name": "POTASSIUM BROMIDE", "strength": "9 [hp_C]/9[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}