Package 0220-2113-41

Brand: ferrum sulphuricum

Generic: ferrous sulfate
NDC Package

Package Facts

Identity

Package NDC 0220-2113-41
Digits Only 0220211341
Product NDC 0220-2113
Description

200 [kp_C] in 1 TUBE (0220-2113-41)

Marketing

Marketing Status
Marketed Since 2025-01-01
Brand ferrum sulphuricum
Generic ferrous sulfate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3a749d62-0e21-0c15-e063-6394a90ac1a8", "openfda": {"unii": ["39R4TAN1VT"], "spl_set_id": ["3a749d62-0e20-0c15-e063-6394a90ac1a8"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-2113-41)", "package_ndc": "0220-2113-41", "marketing_start_date": "20250101"}], "brand_name": "FERRUM SULPHURICUM", "product_id": "0220-2113_3a749d62-0e21-0c15-e063-6394a90ac1a8", "dosage_form": "PELLET", "product_ndc": "0220-2113", "generic_name": "FERROUS SULFATE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "FERRUM SULPHURICUM", "active_ingredients": [{"name": "FERROUS SULFATE", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20250101", "listing_expiration_date": "20261231"}