Package 0220-5336-41

Brand: xanthoxylum fraxineum

Generic: zanthoxylum americanum bark
NDC Package

Package Facts

Identity

Package NDC 0220-5336-41
Digits Only 0220533641
Product NDC 0220-5336
Description

200 [kp_C] in 1 TUBE (0220-5336-41)

Marketing

Marketing Status
Marketed Since 2025-01-01
Brand xanthoxylum fraxineum
Generic zanthoxylum americanum bark
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3a0db5f6-4fa6-23bb-e063-6294a90abdf5", "openfda": {"unii": ["A4KL1HMZ7T"], "spl_set_id": ["3a0db5f6-4fa5-23bb-e063-6294a90abdf5"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-5336-41)", "package_ndc": "0220-5336-41", "marketing_start_date": "20250101"}], "brand_name": "XANTHOXYLUM FRAXINEUM", "product_id": "0220-5336_3a0db5f6-4fa6-23bb-e063-6294a90abdf5", "dosage_form": "PELLET", "product_ndc": "0220-5336", "generic_name": "ZANTHOXYLUM AMERICANUM BARK", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "XANTHOXYLUM FRAXINEUM", "active_ingredients": [{"name": "ZANTHOXYLUM AMERICANUM BARK", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20250101", "listing_expiration_date": "20261231"}