Package 0220-5200-41

Brand: veratrum album

Generic: veratrum album root
NDC Package

Package Facts

Identity

Package NDC 0220-5200-41
Digits Only 0220520041
Product NDC 0220-5200
Description

200 [kp_C] in 1 TUBE (0220-5200-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand veratrum album
Generic veratrum album root
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "044c713e-bd2b-f64b-e063-6394a90a7699", "openfda": {"unii": ["QNS6W5US1Z"], "spl_set_id": ["85e6d900-015d-4b3d-e053-2991aa0a99d0"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-5200-41)", "package_ndc": "0220-5200-41", "marketing_start_date": "19830303"}], "brand_name": "VERATRUM ALBUM", "product_id": "0220-5200_044c713e-bd2b-f64b-e063-6394a90a7699", "dosage_form": "PELLET", "product_ndc": "0220-5200", "generic_name": "VERATRUM ALBUM ROOT", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "VERATRUM ALBUM", "active_ingredients": [{"name": "VERATRUM ALBUM ROOT", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}