Package 0220-0951-41

Brand: bufo rana

Generic: bufo bufo cutaneous gland
NDC Package

Package Facts

Identity

Package NDC 0220-0951-41
Digits Only 0220095141
Product NDC 0220-0951
Description

9 [hp_C] in 1 TUBE (0220-0951-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
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": "09bab28f-d785-f2e7-e063-6294a90a1b79", "openfda": {"unii": ["Q59QU6N72Q"], "spl_set_id": ["848ac763-1839-f6e3-e053-2a91aa0ad805"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "9 [hp_C] in 1 TUBE (0220-0951-41)", "package_ndc": "0220-0951-41", "marketing_start_date": "19830303"}], "brand_name": "Bufo rana", "product_id": "0220-0951_09bab28f-d785-f2e7-e063-6294a90a1b79", "dosage_form": "PELLET", "product_ndc": "0220-0951", "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": "9 [hp_C]/9[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}