Package 0220-0845-41

Brand: berberis vulgaris

Generic: berberis vulgaris root bark
NDC Package

Package Facts

Identity

Package NDC 0220-0845-41
Digits Only 0220084541
Product NDC 0220-0845
Product ID 0220-0845_00edbc64-9d36-5751-e063-6294a90a400b
Description

10 [hp_X] in 1 TUBE (0220-0845-41)

Marketing

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

Linked Drug Pages (1)

Berberis vulgaris ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "00edbc64-9d36-5751-e063-6294a90a400b", "openfda": {"unii": ["1TH8Q20J0U"], "spl_set_id": ["85012034-e095-0a78-e053-2a91aa0a3ee9"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 [hp_X] in 1 TUBE (0220-0845-41)", "package_ndc": "0220-0845-41", "marketing_start_date": "19830303"}], "brand_name": "Berberis vulgaris", "product_id": "0220-0845_00edbc64-9d36-5751-e063-6294a90a400b", "dosage_form": "PELLET", "product_ndc": "0220-0845", "generic_name": "BERBERIS VULGARIS ROOT BARK", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Berberis vulgaris", "active_ingredients": [{"name": "BERBERIS VULGARIS ROOT BARK", "strength": "10 [hp_X]/10[hp_X]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}