Package 0220-0450-41
Brand: arnica montana
Generic: arnica montanaPackage Facts
Identity
Package NDC
0220-0450-41
Digits Only
0220045041
Product NDC
0220-0450
Description
30 [hp_X] in 1 TUBE (0220-0450-41)
Marketing
Marketing Status
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": "472e6cce-65e8-4b84-e063-6394a90a50eb", "openfda": {"unii": ["O80TY208ZW"], "spl_set_id": ["84ef94a8-7a80-1397-e053-2a91aa0a18c3"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_X] in 1 TUBE (0220-0450-41)", "package_ndc": "0220-0450-41", "marketing_start_date": "19830303"}], "brand_name": "Arnica montana", "product_id": "0220-0450_472e6cce-65e8-4b84-e063-6394a90a50eb", "dosage_form": "PELLET", "product_ndc": "0220-0450", "generic_name": "ARNICA MONTANA", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Arnica montana", "active_ingredients": [{"name": "ARNICA MONTANA", "strength": "30 [hp_X]/30[hp_X]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}