Package 0220-2994-41

Brand: laurocerasus

Generic: prunus laurocerasus leaf
NDC Package

Package Facts

Identity

Package NDC 0220-2994-41
Digits Only 0220299441
Product NDC 0220-2994
Description

200 [kp_C] in 1 TUBE (0220-2994-41)

Marketing

Marketing Status
Marketed Since 2025-01-01
Brand laurocerasus
Generic prunus laurocerasus leaf
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3ca86200-7cb5-26f1-e063-6294a90adfc3", "openfda": {"unii": ["F26P2D4757"], "spl_set_id": ["3a89ddc1-1da7-809c-e063-6294a90a1d2d"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-2994-41)", "package_ndc": "0220-2994-41", "marketing_start_date": "20250101"}], "brand_name": "LAUROCERASUS", "product_id": "0220-2994_3ca86200-7cb5-26f1-e063-6294a90adfc3", "dosage_form": "PELLET", "product_ndc": "0220-2994", "generic_name": "PRUNUS LAUROCERASUS LEAF", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "LAUROCERASUS", "active_ingredients": [{"name": "PRUNUS LAUROCERASUS LEAF", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20250101", "listing_expiration_date": "20261231"}