Package 0220-0812-41

Brand: bellis perennis

Generic: bellis perennis
NDC Package

Package Facts

Identity

Package NDC 0220-0812-41
Digits Only 0220081241
Product NDC 0220-0812
Description

6 [hp_C] in 1 TUBE (0220-0812-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand bellis perennis
Generic bellis perennis
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "07d8f0e7-e5f8-1b82-e063-6394a90aa0e5", "openfda": {"unii": ["2HU33I03UY"], "spl_set_id": ["8476f35a-1cc6-307b-e053-2991aa0a4ced"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 [hp_C] in 1 TUBE (0220-0812-41)", "package_ndc": "0220-0812-41", "marketing_start_date": "19830303"}], "brand_name": "Bellis perennis", "product_id": "0220-0812_07d8f0e7-e5f8-1b82-e063-6394a90aa0e5", "dosage_form": "PELLET", "product_ndc": "0220-0812", "generic_name": "BELLIS PERENNIS", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Bellis perennis", "active_ingredients": [{"name": "BELLIS PERENNIS", "strength": "6 [hp_C]/6[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}