Package 0220-5485-41

Brand: zincum sulphuricum

Generic: zinc sulfate heptahydrate
NDC Package

Package Facts

Identity

Package NDC 0220-5485-41
Digits Only 0220548541
Product NDC 0220-5485
Product ID 0220-5485_0a36c585-782c-7493-e063-6394a90aecbb
Description

30 [hp_C] in 1 TUBE (0220-5485-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand zincum sulphuricum
Generic zinc sulfate heptahydrate
Sample Package No

Linked Drug Pages (1)

ZINCUM SULPHURICUM ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0a36c585-782c-7493-e063-6394a90aecbb", "openfda": {"unii": ["N57JI2K7WP"], "spl_set_id": ["8506f6c4-0c62-ebe6-e053-2a91aa0a8561"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-5485-41)", "package_ndc": "0220-5485-41", "marketing_start_date": "19830303"}], "brand_name": "ZINCUM SULPHURICUM", "product_id": "0220-5485_0a36c585-782c-7493-e063-6394a90aecbb", "dosage_form": "PELLET", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "0220-5485", "generic_name": "ZINC SULFATE HEPTAHYDRATE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ZINCUM SULPHURICUM", "active_ingredients": [{"name": "ZINC SULFATE HEPTAHYDRATE", "strength": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}