Package 0220-1231-41

Brand: ceanothus americanus

Generic: ceanothus americanus leaf
NDC Package

Package Facts

Identity

Package NDC 0220-1231-41
Digits Only 0220123141
Product NDC 0220-1231
Description

30 [hp_C] in 1 TUBE (0220-1231-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand ceanothus americanus
Generic ceanothus americanus leaf
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "09bef660-9f66-48d2-e063-6394a90a2104", "openfda": {"unii": ["25B1Y14T8N"], "spl_set_id": ["6c4427cd-432c-d1b3-e053-2991aa0a0f36"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-1231-41)", "package_ndc": "0220-1231-41", "marketing_start_date": "19830303"}], "brand_name": "Ceanothus americanus", "product_id": "0220-1231_09bef660-9f66-48d2-e063-6394a90a2104", "dosage_form": "PELLET", "product_ndc": "0220-1231", "generic_name": "CEANOTHUS AMERICANUS LEAF", "labeler_name": "Boiron", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ceanothus americanus", "active_ingredients": [{"name": "CEANOTHUS AMERICANUS LEAF", "strength": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}