Package 0220-5275-41

Brand: vipera berus

Generic: vipera berus venom
NDC Package

Package Facts

Identity

Package NDC 0220-5275-41
Digits Only 0220527541
Product NDC 0220-5275
Description

200 [kp_C] in 1 TUBE (0220-5275-41)

Marketing

Marketing Status
Marketed Since 2024-01-01
Brand vipera berus
Generic vipera berus venom
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0c070987-c605-7b3b-e063-6294a90ad9de", "openfda": {"unii": ["0ORO6NCA4M"], "spl_set_id": ["0c070987-c604-7b3b-e063-6294a90ad9de"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-5275-41)", "package_ndc": "0220-5275-41", "marketing_start_date": "20240101"}], "brand_name": "VIPERA BERUS", "product_id": "0220-5275_0c070987-c605-7b3b-e063-6294a90ad9de", "dosage_form": "PELLET", "product_ndc": "0220-5275", "generic_name": "VIPERA BERUS VENOM", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "VIPERA BERUS", "active_ingredients": [{"name": "VIPERA BERUS VENOM", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20240101", "listing_expiration_date": "20261231"}