Package 0220-2164-41

Brand: fucus vesiculosus

Generic: fucus vesiculosus
NDC Package

Package Facts

Identity

Package NDC 0220-2164-41
Digits Only 0220216441
Product NDC 0220-2164
Description

200 [kp_C] in 1 TUBE (0220-2164-41)

Marketing

Marketing Status
Marketed Since 2024-01-01
Brand fucus vesiculosus
Generic fucus vesiculosus
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1b19b48b-52ab-7a7b-e063-6294a90abfd5", "openfda": {"unii": ["535G2ABX9M"], "spl_set_id": ["1b18895e-8ed4-675a-e063-6294a90a86a1"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-2164-41)", "package_ndc": "0220-2164-41", "marketing_start_date": "20240101"}], "brand_name": "Fucus vesiculosus", "product_id": "0220-2164_1b19b48b-52ab-7a7b-e063-6294a90abfd5", "dosage_form": "PELLET", "product_ndc": "0220-2164", "generic_name": "FUCUS VESICULOSUS", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Fucus vesiculosus", "active_ingredients": [{"name": "FUCUS VESICULOSUS", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20240101", "listing_expiration_date": "20261231"}