Package 0220-0853-41

Brand: berberis aquifolium

Generic: berberis aquifolium root bark
NDC Package

Package Facts

Identity

Package NDC 0220-0853-41
Digits Only 0220085341
Product NDC 0220-0853
Product ID 0220-0853_3b3c96d0-56f1-2278-e063-6394a90a5c36
Description

200 [kp_C] in 1 TUBE (0220-0853-41)

Marketing

Marketing Status
Marketed Since 2025-01-01
Brand berberis aquifolium
Generic berberis aquifolium root bark
Sample Package No

Linked Drug Pages (1)

BERBERIS AQUIFOLIUM ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3b3c96d0-56f1-2278-e063-6394a90a5c36", "openfda": {"unii": ["VZJ9F3C3SB"], "spl_set_id": ["3b3c96d0-56f0-2278-e063-6394a90a5c36"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-0853-41)", "package_ndc": "0220-0853-41", "marketing_start_date": "20250101"}], "brand_name": "BERBERIS AQUIFOLIUM", "product_id": "0220-0853_3b3c96d0-56f1-2278-e063-6394a90a5c36", "dosage_form": "PELLET", "product_ndc": "0220-0853", "generic_name": "BERBERIS AQUIFOLIUM ROOT BARK", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "BERBERIS AQUIFOLIUM", "active_ingredients": [{"name": "BERBERIS AQUIFOLIUM ROOT BARK", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20250101", "listing_expiration_date": "20261231"}