Package 0220-4382-41

Brand: rhododendron chrysanthum

Generic: rhododendron aureum leaf
NDC Package

Package Facts

Identity

Package NDC 0220-4382-41
Digits Only 0220438241
Product NDC 0220-4382
Description

200 [kp_C] in 1 TUBE (0220-4382-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand rhododendron chrysanthum
Generic rhododendron aureum leaf
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0a21ae0e-36f7-e4cd-e063-6394a90ae089", "openfda": {"unii": ["IV92NQJ73U"], "spl_set_id": ["86ab6364-a0fc-4ccc-e053-2991aa0ab4a0"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-4382-41)", "package_ndc": "0220-4382-41", "marketing_start_date": "19830303"}], "brand_name": "Rhododendron chrysanthum", "product_id": "0220-4382_0a21ae0e-36f7-e4cd-e063-6394a90ae089", "dosage_form": "PELLET", "product_ndc": "0220-4382", "generic_name": "RHODODENDRON AUREUM LEAF", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Rhododendron chrysanthum", "active_ingredients": [{"name": "RHODODENDRON AUREUM LEAF", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}