Package 0220-0945-41

Brand: bryonia

Generic: bryonia alba root
NDC Package

Package Facts

Identity

Package NDC 0220-0945-41
Digits Only 0220094541
Product NDC 0220-0945
Description

200 [kp_C] in 1 TUBE (0220-0945-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand bryonia
Generic bryonia alba root
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47a9fe22-73df-3c2d-e063-6394a90aa100", "openfda": {"unii": ["T7J046YI2B"], "spl_set_id": ["85023f1e-dfb2-3261-e053-2991aa0aa9f7"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-0945-41)", "package_ndc": "0220-0945-41", "marketing_start_date": "19830303"}], "brand_name": "Bryonia", "product_id": "0220-0945_47a9fe22-73df-3c2d-e063-6394a90aa100", "dosage_form": "PELLET", "product_ndc": "0220-0945", "generic_name": "BRYONIA ALBA ROOT", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Bryonia", "active_ingredients": [{"name": "BRYONIA ALBA ROOT", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20271231"}