Package 0220-0606-41

Brand: artemisia vulgaris

Generic: artemisia vulgaris root
NDC Package

Package Facts

Identity

Package NDC 0220-0606-41
Digits Only 0220060641
Product NDC 0220-0606
Description

200 [kp_C] in 1 TUBE (0220-0606-41)

Marketing

Marketing Status
Marketed Since 2024-01-01
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": "253c9d92-7556-4429-e063-6394a90a52f1", "openfda": {"unii": ["32MP823R8S"], "spl_set_id": ["253c9d92-7555-4429-e063-6394a90a52f1"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-0606-41)", "package_ndc": "0220-0606-41", "marketing_start_date": "20240101"}], "brand_name": "Artemisia vulgaris", "product_id": "0220-0606_253c9d92-7556-4429-e063-6394a90a52f1", "dosage_form": "PELLET", "product_ndc": "0220-0606", "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": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20240101", "listing_expiration_date": "20261231"}