Package 0220-0774-41

Brand: baptisia tinctoria

Generic: baptisia tinctoria root
NDC Package

Package Facts

Identity

Package NDC 0220-0774-41
Digits Only 0220077441
Product NDC 0220-0774
Description

9 [hp_C] in 1 TUBE (0220-0774-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand baptisia tinctoria
Generic baptisia tinctoria root
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "09ba5762-6b48-3a9b-e063-6394a90a53e9", "openfda": {"unii": ["5EF0HWI5WU"], "spl_set_id": ["8463230e-bcce-0eb2-e053-2a91aa0ad584"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "9 [hp_C] in 1 TUBE (0220-0774-41)", "package_ndc": "0220-0774-41", "marketing_start_date": "19830303"}], "brand_name": "Baptisia tinctoria", "product_id": "0220-0774_09ba5762-6b48-3a9b-e063-6394a90a53e9", "dosage_form": "PELLET", "product_ndc": "0220-0774", "generic_name": "BAPTISIA TINCTORIA ROOT", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Baptisia tinctoria", "active_ingredients": [{"name": "BAPTISIA TINCTORIA ROOT", "strength": "9 [hp_C]/9[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}