Package 0220-0949-41
Brand: bryonia
Generic: bryonia alba rootPackage Facts
Identity
Package NDC
0220-0949-41
Digits Only
0220094941
Product NDC
0220-0949
Description
30 [hp_X] in 1 TUBE (0220-0949-41)
Marketing
Marketing Status
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": "47aa1836-3946-0917-e063-6294a90a652f", "openfda": {"unii": ["T7J046YI2B"], "spl_set_id": ["8502ac84-1022-e92d-e053-2991aa0a38bc"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_X] in 1 TUBE (0220-0949-41)", "package_ndc": "0220-0949-41", "marketing_start_date": "19830303"}], "brand_name": "Bryonia", "product_id": "0220-0949_47aa1836-3946-0917-e063-6294a90a652f", "dosage_form": "PELLET", "product_ndc": "0220-0949", "generic_name": "BRYONIA ALBA ROOT", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Bryonia", "active_ingredients": [{"name": "BRYONIA ALBA ROOT", "strength": "30 [hp_X]/30[hp_X]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20271231"}