Package 0220-2307-41

Brand: gnaphalium polycephalum

Generic: pseudognaphalium obtusifolium
NDC Package

Package Facts

Identity

Package NDC 0220-2307-41
Digits Only 0220230741
Product NDC 0220-2307
Product ID 0220-2307_0a0d563e-f71c-b11c-e063-6294a90ababb
Description

200 [kp_C] in 1 TUBE (0220-2307-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand gnaphalium polycephalum
Generic pseudognaphalium obtusifolium
Sample Package No

Linked Drug Pages (1)

Gnaphalium polycephalum ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0a0d563e-f71c-b11c-e063-6294a90ababb", "openfda": {"unii": ["36XQ854NWW"], "spl_set_id": ["85a4d643-51e5-99c2-e053-2a91aa0a5fe2"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-2307-41)", "package_ndc": "0220-2307-41", "marketing_start_date": "19830303"}], "brand_name": "Gnaphalium polycephalum", "product_id": "0220-2307_0a0d563e-f71c-b11c-e063-6294a90ababb", "dosage_form": "PELLET", "product_ndc": "0220-2307", "generic_name": "PSEUDOGNAPHALIUM OBTUSIFOLIUM", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Gnaphalium polycephalum", "active_ingredients": [{"name": "PSEUDOGNAPHALIUM OBTUSIFOLIUM", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}