FDA.reportPublic FDA data

Lithium Sulphuratum

Product NDC
37662-3757
Requested package NDC
37662-3757-2
11-digit product format
376623757
Labeler code
37662
Product ID
37662-3757_03280bb4-794e-57bb-e063-6394a90a854f
Type
HUMAN OTC DRUG
Nonproprietary name
Lithium Sulphuratum
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2023-08-17
Substance
LITHIUM SULFATE
Active strength
200 [hp_C]/1
Pharmacologic classes
Mood Stabilizer [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Lithium Sulphuratum
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
LITHIUM SULFATE200 [hp_C]/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
919XA137JKInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
03280bb4-794d-57bb-e063-6394a90a854fAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
b3053bb1-353b-4a0b-bca5-28fe7228957cProduct name220250124
8ce6e144-236f-b7be-f690-f06e0c8c6bd3Product name220170725
f09af6ee-c6dd-d0ce-77ad-93508bcdacedProduct name420161205

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-3757-1Lithium Sulphuratum200 in 1 VIAL, GLASSPELLET2001
37662-3757-2Lithium Sulphuratum500 in 1 VIAL, GLASSPELLET5001
37662-3757-3Lithium Sulphuratum3000 in 1 BOTTLE, GLASSPELLET30001
37662-3757-4Lithium Sulphuratum10000 in 1 BOTTLE, GLASSPELLET100001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-3757LITHIUM SULPHURATUM PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, 4 package rows20230818_03280bb4-794d-57bb-e063-6394a90a854f.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
Lithium SulphuratumLITHIUM SULPHURATUMHahnemann Laboratories, INC.03280bb4-794d-57bb-e063-6394a90a854f2023-08-17Exact identifier
ndc (package): 37662-3757-2
ndc (product): 37662-3757
ndc11 (package): 37662375702

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
37662-3757-237662375702500 PELLET in 1 VIAL, GLASS (37662-3757-2) 500 pellet2023-08-17NoNoCurrent