Package 0220-1541-41
Brand: corallium rubrum
Generic: corallium rubrum exoskeletonPackage Facts
Identity
Package NDC
0220-1541-41
Digits Only
0220154141
Product NDC
0220-1541
Description
5 [hp_C] in 1 TUBE (0220-1541-41)
Marketing
Marketing Status
Brand
corallium rubrum
Generic
corallium rubrum exoskeleton
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0a0c373a-4961-0591-e063-6294a90a8983", "openfda": {"unii": ["2CA71K0DLE"], "spl_set_id": ["7a2d4904-d2b1-ef74-e053-2a91aa0a284a"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 [hp_C] in 1 TUBE (0220-1541-41)", "package_ndc": "0220-1541-41", "marketing_start_date": "19830303"}], "brand_name": "Corallium rubrum", "product_id": "0220-1541_0a0c373a-4961-0591-e063-6294a90a8983", "dosage_form": "PELLET", "product_ndc": "0220-1541", "generic_name": "CORALLIUM RUBRUM EXOSKELETON", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Corallium rubrum", "active_ingredients": [{"name": "CORALLIUM RUBRUM EXOSKELETON", "strength": "5 [hp_C]/5[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}