FDA.reportPublic FDA data

FERRUM PHOSPHATE

Product NDC
54973-3431
Requested package NDC
54973-3431-2
11-digit product format
549733431
Labeler code
54973
Product ID
54973-3431_f030e9fc-1ece-b915-e053-2a95a90a5356
Type
HUMAN OTC DRUG
Nonproprietary name
sodium phosphate
Dosage form
TABLET
Route
ORAL
Labeler
Hyland's Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1940-01-01
Substance
SODIUM PHOSPHATE
Active strength
6 [hp_X]/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage54973-343154973-3431-2DDiscontinued by firm2026-08-11

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 · 12 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-100efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09557ba5c1ecfa…9c80585c8c6e…

Additional Listing Data#

Finished product
Yes
Brand name base
FERRUM PHOSPHATE
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SODIUM PHOSPHATE6 [hp_X]/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
SE337SVY37Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
c114cbad-11ed-4b1c-8ee0-33327c0e1718Available 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
54973-3431-1FERRUM PHOSPHATE500 in 1 BOTTLE, PLASTICTABLET5004
54973-3431-2FERRUM PHOSPHATE1000 in 1 BOTTLE, PLASTICTABLET10004
54973-3431-3FERRUM PHOSPHATE250 in 1 BOTTLE, PLASTICTABLET2504

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
SODIUM PHOSPHATEACTIVE INGREDIENTSE337SVY37FERRUM PHOSPHATE (SODIUM PHOSPHATE) TABLET [HYLAND'S]1
PHOSPHATE IONACTIVE MOIETYNK08V8K8HRFERRUM PHOSPHATE (SODIUM PHOSPHATE) TABLET [HYLAND'S]1
ACACIAINACTIVE INGREDIENT5C5403N26OFERRUM PHOSPHATE (SODIUM PHOSPHATE) TABLET [HYLAND'S]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GFERRUM PHOSPHATE (SODIUM PHOSPHATE) TABLET [HYLAND'S]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54973-3431FERRUM PHOSPHATE (SODIUM PHOSPHATE) TABLET [HYLAND'S INC.]4Current NDC, Legacy NDC, 3 package rows20221220_c114cbad-11ed-4b1c-8ee0-33327c0e1718.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
FERRUM PHOSPHATESODIUM PHOSPHATEHyland's Inc.c114cbad-11ed-4b1c-8ee0-33327c0e17182022-12-19WarningsExact identifier
ndc (package): 54973-3431-2
ndc (product): 54973-3431
ndc11 (package): 54973343102

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
54973-3431-2549733431021000 TABLET in 1 BOTTLE, PLASTIC (54973-3431-2) 1000 tablet1940-01-010000-00-00NoNoCurrent