Package 0220-2396-41

Brand: hekla lava

Generic: hekla lava
NDC Package

Package Facts

Identity

Package NDC 0220-2396-41
Digits Only 0220239641
Product NDC 0220-2396
Description

1 [hp_M] in 1 TUBE (0220-2396-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand hekla lava
Generic hekla lava
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f6003033-dd85-0c03-e053-2995a90a1da7", "openfda": {"unii": ["C21158IIRK"], "spl_set_id": ["87253c3d-8f13-1c73-e053-2991aa0afa15"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 [hp_M] in 1 TUBE (0220-2396-41)", "package_ndc": "0220-2396-41", "marketing_start_date": "19830303"}], "brand_name": "Hekla lava", "product_id": "0220-2396_f6003033-dd85-0c03-e053-2995a90a1da7", "dosage_form": "PELLET", "product_ndc": "0220-2396", "generic_name": "HEKLA LAVA", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Hekla lava", "active_ingredients": [{"name": "HEKLA LAVA", "strength": "1 [hp_M]/[hp_M]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}