FDA.reportPublic FDA data

Ammonium Phosphoricum

Product NDC
37662-3632
11-digit product format
376623632
Labeler code
37662
Product ID
37662-3632_00682d09-bf61-7d6f-e063-6294a90a866b
Type
HUMAN OTC DRUG
Nonproprietary name
Ammonium Phosphoricum
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2023-07-13
Substance
AMMONIUM PHOSPHATE, DIBASIC
Active strength
6 [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
Ammonium Phosphoricum
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AMMONIUM PHOSPHATE, DIBASIC6 [hp_C]/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
10LGE70FSUInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
00682d09-bf60-7d6f-e063-6294a90a866bAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
efd58dcf-540a-4531-8766-e713129ca6f2Product name120250307
4b7700e3-6e0e-45e5-9d22-6f754d61386eProduct name220250304
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-3632-1Ammonium Phosphoricum200 in 1 VIAL, GLASSPELLET2001
37662-3632-2Ammonium Phosphoricum1200 in 1 BOTTLE, GLASSPELLET12001
37662-3632-3Ammonium Phosphoricum4000 in 1 BOTTLE, GLASSPELLET40001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-3632AMMONIUM PHOSPHORICUM PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, 3 package rows20230714_00682d09-bf60-7d6f-e063-6294a90a866b.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
Ammonium PhosphoricumAMMONIUM PHOSPHORICUMHahnemann Laboratories, INC.00682d09-bf60-7d6f-e063-6294a90a866b2023-07-13Exact identifier
ndc (product): 37662-3632

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
37662-3632-137662363201200 PELLET in 1 VIAL, GLASS (37662-3632-1) 200 pellet2023-07-13NoNoCurrent
37662-3632-2376623632021200 PELLET in 1 BOTTLE, GLASS (37662-3632-2) 1200 pellet2023-07-13NoNoCurrent
37662-3632-3376623632034000 PELLET in 1 BOTTLE, GLASS (37662-3632-3) 4000 pellet2023-07-13NoNoCurrent