ferrous sulfate

Generic: ferrous sulfate

Labeler: richmond pharmaceuticals, inc.
NDC Directory HUMAN OTC DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name ferrous sulfate
Generic Name ferrous sulfate
Labeler richmond pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

ferrous sulfate 325 mg/1

Manufacturer
Richmond Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 54738-963
Product ID 54738-963_2a327c66-d561-6a9b-e063-6294a90a5d0a
Product Type HUMAN OTC DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2015-06-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 54738963
Hyphenated Format 54738-963

Supplemental Identifiers

RxCUI
310325
UNII
39R4TAN1VT

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 ferrous sulfate (source: ndc)
Generic Name ferrous sulfate (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (54738-963-01)
  • 1000 TABLET in 1 BOTTLE (54738-963-03)
source: ndc

Packages (2)

Ingredients (1)

ferrous sulfate (325 mg/1)

Linked Drug Pages (2)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a327c66-d561-6a9b-e063-6294a90a5d0a", "openfda": {"unii": ["39R4TAN1VT"], "rxcui": ["310325"], "spl_set_id": ["58dd4f30-980b-44bc-9f8e-8d4626854b91"], "manufacturer_name": ["Richmond Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (54738-963-01)", "package_ndc": "54738-963-01", "marketing_start_date": "20150601"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (54738-963-03)", "package_ndc": "54738-963-03", "marketing_start_date": "20150601"}], "brand_name": "FERROUS SULFATE", "product_id": "54738-963_2a327c66-d561-6a9b-e063-6294a90a5d0a", "dosage_form": "TABLET", "product_ndc": "54738-963", "generic_name": "FERROUS SULFATE", "labeler_name": "Richmond Pharmaceuticals, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "FERROUS SULFATE", "active_ingredients": [{"name": "FERROUS SULFATE", "strength": "325 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20150601", "listing_expiration_date": "20261231"}