ferrum phosphate

Generic: sodium phosphate

Labeler: hyland's inc.
NDC Directory HUMAN OTC DRUG UNAPPROVED HOMEOPATHIC Inactive Finished

Drug Facts

Product Profile

Brand Name ferrum phosphate
Generic Name sodium phosphate
Labeler hyland's inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sodium phosphate 6 [hp_X]/1

Manufacturer
Hyland's Inc.

Identifiers & Regulatory

Product NDC 54973-3431
Product ID 54973-3431_f030e9fc-1ece-b915-e053-2a95a90a5356
Product Type HUMAN OTC DRUG
Marketing Category UNAPPROVED HOMEOPATHIC
Listing Expiration 2026-12-31
Marketing Start 1940-01-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 549733431
Hyphenated Format 54973-3431

Supplemental Identifiers

UPC
0354973343115
UNII
SE337SVY37

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name ferrum phosphate (source: ndc)
Generic Name sodium phosphate (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 6 [hp_X]/1
source: ndc
Packaging
  • 500 TABLET in 1 BOTTLE, PLASTIC (54973-3431-1)
source: ndc

Packages (1)

Ingredients (1)

sodium phosphate (6 [hp_X]/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f030e9fc-1ece-b915-e053-2a95a90a5356", "openfda": {"upc": ["0354973343115"], "unii": ["SE337SVY37"], "spl_set_id": ["c114cbad-11ed-4b1c-8ee0-33327c0e1718"], "manufacturer_name": ["Hyland's Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (54973-3431-1)", "package_ndc": "54973-3431-1", "marketing_start_date": "19400101"}], "brand_name": "FERRUM PHOSPHATE", "product_id": "54973-3431_f030e9fc-1ece-b915-e053-2a95a90a5356", "dosage_form": "TABLET", "product_ndc": "54973-3431", "generic_name": "sodium phosphate", "labeler_name": "Hyland's Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "FERRUM PHOSPHATE", "active_ingredients": [{"name": "SODIUM PHOSPHATE", "strength": "6 [hp_X]/1"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19400101", "listing_expiration_date": "20261231"}