Package 0220-0939-41

Brand: bryonia

Generic: bryonia alba root
NDC Package

Package Facts

Identity

Package NDC 0220-0939-41
Digits Only 0220093941
Product NDC 0220-0939
Description

5 [hp_C] in 1 TUBE (0220-0939-41)

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": "47aa69cd-c9e6-8485-e063-6294a90a1710", "openfda": {"unii": ["T7J046YI2B"], "spl_set_id": ["848996a1-46e4-035f-e053-2a91aa0a5822"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 [hp_C] in 1 TUBE (0220-0939-41)", "package_ndc": "0220-0939-41", "marketing_start_date": "19830303"}], "brand_name": "Bryonia", "product_id": "0220-0939_47aa69cd-c9e6-8485-e063-6294a90a1710", "dosage_form": "PELLET", "product_ndc": "0220-0939", "generic_name": "BRYONIA ALBA ROOT", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Bryonia", "active_ingredients": [{"name": "BRYONIA ALBA ROOT", "strength": "5 [hp_C]/5[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20271231"}