Package 0220-0733-41

Brand: bellis perennis

Generic: bellis perennis
NDC Package

Package Facts

Identity

Package NDC 0220-0733-41
Digits Only 0220073341
Product NDC 0220-0733
Description

200 [kp_C] in 1 TUBE (0220-0733-41)

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": "f7faf93a-da02-cd48-e053-6394a90a5af4", "openfda": {"unii": ["2HU33I03UY"], "spl_set_id": ["850084c3-1dbd-eb8d-e053-2a91aa0a130b"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-0733-41)", "package_ndc": "0220-0733-41", "marketing_start_date": "19830303"}], "brand_name": "Bellis perennis", "product_id": "0220-0733_f7faf93a-da02-cd48-e053-6394a90a5af4", "dosage_form": "PELLET", "product_ndc": "0220-0733", "generic_name": "BELLIS PERENNIS", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Bellis perennis", "active_ingredients": [{"name": "BELLIS PERENNIS", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}