ferrous sulfate
Generic: ferrous sulfate
Labeler: richmond pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
ferrous sulfate
Generic Name
ferrous sulfate
Labeler
richmond pharmaceuticals, inc.
Dosage Form
TABLET
Routes
Active Ingredients
ferrous sulfate 325 mg/1
Manufacturer
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
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 325 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (54738-963-01)
- 1000 TABLET in 1 BOTTLE (54738-963-03)
Packages (2)
Ingredients (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"}