Cuprum Phosphoricum

Product NDC
37662-2234
Requested package NDC
37662-2234-1
11-digit product format
376622234
Labeler code
37662
Product ID
37662-2234_f166517a-76d5-cc19-e053-2995a90ae4f1
Type
HUMAN OTC DRUG
Nonproprietary name
Cuprum Phosphoricum
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2023-01-03
Substance
CUPRIC PHOSPHATE
Active strength
500 [hp_C]/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product
Yes
Brand name base
Cuprum Phosphoricum
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CUPRIC PHOSPHATE500 [hp_C]/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
N8NP6FR80RInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
f166517a-76d4-cc19-e053-2995a90ae4f1Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-2234-1Cuprum Phosphoricum200 in 1 VIAL, GLASSPELLET2001
37662-2234-2Cuprum Phosphoricum500 in 1 VIAL, GLASSPELLET5001
37662-2234-3Cuprum Phosphoricum3000 in 1 BOTTLE, GLASSPELLET30001
37662-2234-4Cuprum Phosphoricum10000 in 1 BOTTLE, GLASSPELLET100001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-2234CUPRUM PHOSPHORICUM PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, Legacy NDC, 4 package rows20230105_f166517a-76d4-cc19-e053-2995a90ae4f1.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Cuprum PhosphoricumCUPRUM PHOSPHORICUMHahnemann Laboratories, INC.f166517a-76d4-cc19-e053-2995a90ae4f12023-01-03Exact identifier
ndc (package): 37662-2234-1
ndc (product): 37662-2234
ndc11 (package): 37662223401

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
37662-2234-137662223401200 PELLET in 1 VIAL, GLASS (37662-2234-1) 200 pellet2023-01-030000-00-00NoNoCurrent