FDA.reportPublic FDA data

Ammonium Phosphoricum

Product NDC
63545-957
11-digit product format
635450957
Labeler code
63545
Product ID
63545-957_2b49322a-dc24-f4a1-e063-6294a90a6cff
Type
HUMAN OTC DRUG
Nonproprietary name
Ammonium Phosphoricum
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2020-10-23
Substance
AMMONIUM PHOSPHATE, DIBASIC
Active strength
30 [hp_C]/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 15 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2022-08-30 03:57 UTC · source 2022-08-29excluded productproductfb8cb913e6d1…eb8c232b6be0…
2022-08-30 03:57 UTC · source 2022-08-29excluded packagepackage63545-957-04fb8cb913e6d1…eb8c232b6be0…
2022-08-30 03:57 UTC · source 2022-08-29excluded packagepackage63545-957-02fb8cb913e6d1…eb8c232b6be0…
2022-08-30 03:57 UTC · source 2022-08-29excluded packagepackage63545-957-03fb8cb913e6d1…eb8c232b6be0…
2022-08-30 03:57 UTC · source 2022-08-29excluded packagepackage63545-957-01fb8cb913e6d1…eb8c232b6be0…
2022-04-09 23:13 UTC · source 2022-04-08excluded productproduct86f5da6cb304…a595104c45d7…
2022-04-09 23:13 UTC · source 2022-04-08excluded packagepackage63545-957-0486f5da6cb304…a595104c45d7…
2022-04-09 23:13 UTC · source 2022-04-08excluded packagepackage63545-957-0286f5da6cb304…a595104c45d7…
2022-04-09 23:13 UTC · source 2022-04-08excluded packagepackage63545-957-0386f5da6cb304…a595104c45d7…
2022-04-09 23:13 UTC · source 2022-04-08excluded packagepackage63545-957-0186f5da6cb304…a595104c45d7…
2022-04-04 05:40 UTC · source 2022-04-01excluded productproductbd6a592717d7…303034d00443…
2022-04-04 05:40 UTC · source 2022-04-01excluded packagepackage63545-957-04bd6a592717d7…303034d00443…
2022-04-04 05:40 UTC · source 2022-04-01excluded packagepackage63545-957-02bd6a592717d7…303034d00443…
2022-04-04 05:40 UTC · source 2022-04-01excluded packagepackage63545-957-03bd6a592717d7…303034d00443…
2022-04-04 05:40 UTC · source 2022-04-01excluded packagepackage63545-957-01bd6a592717d7…303034d00443…

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AMMONIUM PHOSPHATE, DIBASIC30 [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
b25e39bd-7e81-1ef1-e053-2995a90a6d82Available 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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
63545-957-012022-12-12b25e39bd-7e81-1ef1-e053-2995a90a6d82
63545-957-022022-12-12b25e39bd-7e81-1ef1-e053-2995a90a6d82
63545-957-032022-12-12b25e39bd-7e81-1ef1-e053-2995a90a6d82
63545-957-042022-12-12b25e39bd-7e81-1ef1-e053-2995a90a6d82
63545-957-012022-01-28b25e39bd-7e81-1ef1-e053-2995a90a6d82
63545-957-022022-01-28b25e39bd-7e81-1ef1-e053-2995a90a6d82
63545-957-032022-01-28b25e39bd-7e81-1ef1-e053-2995a90a6d82
63545-957-042022-01-28b25e39bd-7e81-1ef1-e053-2995a90a6d82

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63545-957-01Ammonium Phosphoricum80 in 1 VIAL, GLASSPELLET803
63545-957-02Ammonium Phosphoricum200 in 1 VIAL, GLASSPELLET2003
63545-957-03Ammonium Phosphoricum1200 in 1 BOTTLE, GLASSPELLET12003
63545-957-04Ammonium Phosphoricum4000 in 1 BOTTLE, GLASSPELLET40003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63545-957AMMONIUM PHOSPHORICUM PELLET [HAHNEMANN LABORATORIES, INC.]3Current NDC, Legacy NDC, 4 package rows20250112_b25e39bd-7e81-1ef1-e053-2995a90a6d82.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.b25e39bd-7e81-1ef1-e053-2995a90a6d822025-01-09Exact identifier
ndc (product): 63545-957

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63545-957-016354509570180 PELLET in 1 VIAL, GLASS (63545-957-01) 80 pellet2020-10-230000-00-00NoNoCurrent
63545-957-0263545095702200 PELLET in 1 VIAL, GLASS (63545-957-02) 200 pellet2020-10-230000-00-00NoNoCurrent
63545-957-03635450957031200 PELLET in 1 BOTTLE, GLASS (63545-957-03) 1200 pellet2020-10-230000-00-00NoNoCurrent
63545-957-04635450957044000 PELLET in 1 BOTTLE, GLASS (63545-957-04) 4000 pellet2020-10-230000-00-00NoNoCurrent