Package 0220-2111-41

Brand: ferrum sulphuricum

Generic: ferrous sulfate
NDC Package

Package Facts

Identity

Package NDC 0220-2111-41
Digits Only 0220211141
Product NDC 0220-2111
Description

30 [hp_C] in 1 TUBE (0220-2111-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
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": "0a0cbae3-25d2-6d47-e063-6294a90a0431", "openfda": {"unii": ["39R4TAN1VT"], "spl_set_id": ["7a4087d8-d054-bbdc-e053-2991aa0ae8cf"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-2111-41)", "package_ndc": "0220-2111-41", "marketing_start_date": "19830303"}], "brand_name": "Ferrum sulphuricum", "product_id": "0220-2111_0a0cbae3-25d2-6d47-e063-6294a90a0431", "dosage_form": "PELLET", "product_ndc": "0220-2111", "generic_name": "FERROUS SULFATE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ferrum sulphuricum", "active_ingredients": [{"name": "FERROUS SULFATE", "strength": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}