Package 0220-0954-41
Brand: bufo rana
Generic: bufo bufo cutaneous glandPackage Facts
Identity
Package NDC
0220-0954-41
Digits Only
0220095441
Product NDC
0220-0954
Description
200 [kp_C] in 1 TUBE (0220-0954-41)
Marketing
Marketing Status
Brand
bufo rana
Generic
bufo bufo cutaneous gland
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "09baeb3e-9bcb-696a-e063-6394a90a6497", "openfda": {"unii": ["Q59QU6N72Q"], "spl_set_id": ["8502dbce-7c6f-a630-e053-2a91aa0ab82d"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-0954-41)", "package_ndc": "0220-0954-41", "marketing_start_date": "19830303"}], "brand_name": "Bufo rana", "product_id": "0220-0954_09baeb3e-9bcb-696a-e063-6394a90a6497", "dosage_form": "PELLET", "product_ndc": "0220-0954", "generic_name": "BUFO BUFO CUTANEOUS GLAND", "labeler_name": "Boiron", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bufo rana", "active_ingredients": [{"name": "BUFO BUFO CUTANEOUS GLAND", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}