Package 65111-005-67

Brand: arnica montana

Generic: arnica montana
NDC Package

Package Facts

Identity

Package NDC 65111-005-67
Digits Only 6511100567
Product NDC 65111-005
Description

150 TABLET in 1 BOTTLE (65111-005-67)

Marketing

Marketing Status
Discontinued 2026-09-22
Brand arnica montana
Generic arnica montana
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b3fc45c7-c208-4194-82a2-ad311dce494e", "openfda": {"unii": ["O80TY208ZW"], "spl_set_id": ["a134a2a4-2faa-4ef2-8af1-7f8be420f32b"], "manufacturer_name": ["Vitamedica Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "150 TABLET in 1 BOTTLE (65111-005-67)", "package_ndc": "65111-005-67", "marketing_end_date": "20260922", "marketing_start_date": "20210812"}], "brand_name": "Arnica Montana", "product_id": "65111-005_b3fc45c7-c208-4194-82a2-ad311dce494e", "dosage_form": "TABLET", "product_ndc": "65111-005", "generic_name": "Arnica Montana", "labeler_name": "Vitamedica Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Arnica Montana", "active_ingredients": [{"name": "ARNICA MONTANA", "strength": "30 [hp_X]/1"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_end_date": "20260922", "marketing_start_date": "20210812"}