Package 0220-0734-41

Brand: bellis perennis

Generic: bellis perennis
NDC Package

Package Facts

Identity

Package NDC 0220-0734-41
Digits Only 0220073441
Product NDC 0220-0734
Description

1 [hp_M] in 1 TUBE (0220-0734-41)

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": "09ba5e8f-735b-2a35-e063-6394a90a98d0", "openfda": {"unii": ["2HU33I03UY"], "spl_set_id": ["850084c3-1dd2-eb8d-e053-2a91aa0a130b"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 [hp_M] in 1 TUBE (0220-0734-41)", "package_ndc": "0220-0734-41", "marketing_start_date": "19830303"}], "brand_name": "Bellis perennis", "product_id": "0220-0734_09ba5e8f-735b-2a35-e063-6394a90a98d0", "dosage_form": "PELLET", "product_ndc": "0220-0734", "generic_name": "BELLIS PERENNIS", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Bellis perennis", "active_ingredients": [{"name": "BELLIS PERENNIS", "strength": "1 [hp_M]/[hp_M]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}