Package 0220-0831-41

Brand: berberis aquifolium

Generic: berberis aquifolium root bark
NDC Package

Package Facts

Identity

Package NDC 0220-0831-41
Digits Only 0220083141
Product NDC 0220-0831
Description

30 [hp_C] in 1 TUBE (0220-0831-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand berberis aquifolium
Generic berberis aquifolium root bark
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3bf0f995-f31f-0716-e063-6294a90a1552", "openfda": {"unii": ["VZJ9F3C3SB"], "spl_set_id": ["6c422b8e-fa29-a5b2-e053-2991aa0a27d8"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-0831-41)", "package_ndc": "0220-0831-41", "marketing_start_date": "19830303"}], "brand_name": "Berberis aquifolium", "product_id": "0220-0831_3bf0f995-f31f-0716-e063-6294a90a1552", "dosage_form": "PELLET", "product_ndc": "0220-0831", "generic_name": "BERBERIS AQUIFOLIUM ROOT BARK", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Berberis aquifolium", "active_ingredients": [{"name": "BERBERIS AQUIFOLIUM ROOT BARK", "strength": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}