Package 0220-0775-41

Brand: baptisia tinctoria

Generic: baptisia tinctoria root
NDC Package

Package Facts

Identity

Package NDC 0220-0775-41
Digits Only 0220077541
Product NDC 0220-0775
Description

30 [hp_C] in 1 TUBE (0220-0775-41)

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": "09ba7935-c8f7-d228-e063-6294a90a1e29", "openfda": {"unii": ["5EF0HWI5WU"], "spl_set_id": ["8463bcfa-7155-3b4f-e053-2991aa0a5cb2"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-0775-41)", "package_ndc": "0220-0775-41", "marketing_start_date": "19830303"}], "brand_name": "Baptisia tinctoria", "product_id": "0220-0775_09ba7935-c8f7-d228-e063-6294a90a1e29", "dosage_form": "PELLET", "product_ndc": "0220-0775", "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": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}