Package 73296-019-01
Brand: hypericum perforatum 30x
Generic: hypericum perforatumPackage Facts
Identity
Package NDC
73296-019-01
Digits Only
7329601901
Product NDC
73296-019
Description
4 g in 1 TUBE (73296-019-01)
Marketing
Marketing Status
Brand
hypericum perforatum 30x
Generic
hypericum perforatum
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL", "SUBLINGUAL"], "spl_id": "3593a7ff-b424-dcfe-e063-6394a90ad0af", "openfda": {"unii": ["XK4IUX8MNB"], "spl_set_id": ["3363ee64-2f54-1467-e063-6294a90a2a4d"], "manufacturer_name": ["Laboratoire Schmidt-Nagel Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 g in 1 TUBE (73296-019-01)", "package_ndc": "73296-019-01", "marketing_start_date": "20250501"}], "brand_name": "Hypericum Perforatum 30X", "product_id": "73296-019_3593a7ff-b424-dcfe-e063-6394a90ad0af", "dosage_form": "GLOBULE", "product_ndc": "73296-019", "generic_name": "Hypericum Perforatum", "labeler_name": "Laboratoire Schmidt-Nagel Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Hypericum Perforatum 30X", "active_ingredients": [{"name": "HYPERICUM PERFORATUM WHOLE", "strength": "30 [hp_X]/g"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20250501", "listing_expiration_date": "20261231"}