Package 0220-0609-41

Brand: arum maculatum

Generic: arum maculatum root
NDC Package

Package Facts

Identity

Package NDC 0220-0609-41
Digits Only 0220060941
Product NDC 0220-0609
Description

200 [kp_C] in 1 TUBE (0220-0609-41)

Marketing

Marketing Status
Marketed Since 2024-01-01
Brand arum maculatum
Generic arum maculatum root
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "15ac75cb-ae0f-afb9-e063-6394a90a4679", "openfda": {"unii": ["646O39K8BJ"], "spl_set_id": ["15ac75cb-ae0e-afb9-e063-6394a90a4679"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-0609-41)", "package_ndc": "0220-0609-41", "marketing_start_date": "20240101"}], "brand_name": "Arum maculatum", "product_id": "0220-0609_15ac75cb-ae0f-afb9-e063-6394a90a4679", "dosage_form": "PELLET", "product_ndc": "0220-0609", "generic_name": "ARUM MACULATUM ROOT", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Arum maculatum", "active_ingredients": [{"name": "ARUM MACULATUM ROOT", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20240101", "listing_expiration_date": "20261231"}