Package 0220-0453-41

Brand: arnica montana

Generic: arnica montana
NDC Package

Package Facts

Identity

Package NDC 0220-0453-41
Digits Only 0220045341
Product NDC 0220-0453
Description

200 [hp_X] in 1 TUBE (0220-0453-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand arnica montana
Generic arnica montana
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "471ea0a2-edf5-aa88-e063-6394a90aeede", "openfda": {"unii": ["O80TY208ZW"], "spl_set_id": ["84efa3b9-c595-467f-e053-2991aa0a1008"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [hp_X] in 1 TUBE (0220-0453-41)", "package_ndc": "0220-0453-41", "marketing_start_date": "19830303"}], "brand_name": "Arnica montana", "product_id": "0220-0453_471ea0a2-edf5-aa88-e063-6394a90aeede", "dosage_form": "PELLET", "product_ndc": "0220-0453", "generic_name": "ARNICA MONTANA", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Arnica montana", "active_ingredients": [{"name": "ARNICA MONTANA", "strength": "200 [hp_X]/200[hp_X]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}