Package 0220-4454-41

Brand: rumex crispus

Generic: rumex crispus root
NDC Package

Package Facts

Identity

Package NDC 0220-4454-41
Digits Only 0220445441
Product NDC 0220-4454
Description

6 [hp_C] in 1 TUBE (0220-4454-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand rumex crispus
Generic rumex crispus root
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0868c03c-702d-738d-e063-6394a90a9933", "openfda": {"unii": ["9N1RM2S62C"], "spl_set_id": ["86ba924c-1204-9f60-e053-2991aa0a2fac"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 [hp_C] in 1 TUBE (0220-4454-41)", "package_ndc": "0220-4454-41", "marketing_start_date": "19830303"}], "brand_name": "Rumex crispus", "product_id": "0220-4454_0868c03c-702d-738d-e063-6394a90a9933", "dosage_form": "PELLET", "product_ndc": "0220-4454", "generic_name": "RUMEX CRISPUS ROOT", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Rumex crispus", "active_ingredients": [{"name": "RUMEX CRISPUS ROOT", "strength": "6 [hp_C]/6[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}