Package 54738-963-03

Brand: ferrous sulfate

Generic: ferrous sulfate
NDC Package

Package Facts

Identity

Package NDC 54738-963-03
Digits Only 5473896303
Product NDC 54738-963
Description

1000 TABLET in 1 BOTTLE (54738-963-03)

Marketing

Marketing Status
Marketed Since 2015-06-01
Brand ferrous sulfate
Generic ferrous sulfate
Sample Package No

Linked Drug Pages (1)

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"}