Package 0220-4600-41
Brand: scutellaria lateriflora
Generic: scutellaria lateriflora wholePackage Facts
Identity
Package NDC
0220-4600-41
Digits Only
0220460041
Product NDC
0220-4600
Description
200 [kp_C] in 1 TUBE (0220-4600-41)
Marketing
Marketing Status
Brand
scutellaria lateriflora
Generic
scutellaria lateriflora whole
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3a88b661-0b83-6225-e063-6394a90a18e7", "openfda": {"unii": ["7BP4DH5PDC"], "spl_set_id": ["3a88b661-0b82-6225-e063-6394a90a18e7"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-4600-41)", "package_ndc": "0220-4600-41", "marketing_start_date": "20250101"}], "brand_name": "SCUTELLARIA LATERIFLORA", "product_id": "0220-4600_3a88b661-0b83-6225-e063-6394a90a18e7", "dosage_form": "PELLET", "product_ndc": "0220-4600", "generic_name": "SCUTELLARIA LATERIFLORA WHOLE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SCUTELLARIA LATERIFLORA", "active_ingredients": [{"name": "SCUTELLARIA LATERIFLORA WHOLE", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20250101", "listing_expiration_date": "20261231"}