Package 0220-0552-41
Brand: artemisia vulgaris
Generic: artemisia vulgaris rootPackage Facts
Identity
Package NDC
0220-0552-41
Digits Only
0220055241
Product NDC
0220-0552
Description
30 [hp_C] in 1 TUBE (0220-0552-41)
Marketing
Marketing Status
Brand
artemisia vulgaris
Generic
artemisia vulgaris root
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "253cfb90-3f81-fb07-e063-6294a90a50cf", "openfda": {"unii": ["32MP823R8S"], "spl_set_id": ["6c316c2c-ce7b-a5b2-e053-2991aa0a9743"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-0552-41)", "package_ndc": "0220-0552-41", "marketing_start_date": "19830303"}], "brand_name": "Artemisia vulgaris", "product_id": "0220-0552_253cfb90-3f81-fb07-e063-6294a90a50cf", "dosage_form": "PELLET", "product_ndc": "0220-0552", "generic_name": "ARTEMISIA VULGARIS ROOT", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Artemisia vulgaris", "active_ingredients": [{"name": "ARTEMISIA VULGARIS ROOT", "strength": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}