Package 48951-8356-3

Brand: stannum 30x

Generic: stannum 30x
NDC Package

Package Facts

Identity

Package NDC 48951-8356-3
Digits Only 4895183563
Product NDC 48951-8356
Description

60 mL in 1 BOTTLE, DROPPER (48951-8356-3)

Marketing

Marketing Status
Marketed Since 2009-09-01
Brand stannum 30x
Generic stannum 30x
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "363833fa-b8d3-1093-e063-6394a90a77fc", "openfda": {"unii": ["387GMG9FH5"], "spl_set_id": ["9454572b-643c-6cd1-e053-2a95a90ada1a"], "manufacturer_name": ["Uriel Pharmacy Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 mL in 1 BOTTLE, DROPPER (48951-8356-3)", "package_ndc": "48951-8356-3", "marketing_start_date": "20090901"}], "brand_name": "Stannum 30X", "product_id": "48951-8356_363833fa-b8d3-1093-e063-6394a90a77fc", "dosage_form": "LIQUID", "product_ndc": "48951-8356", "generic_name": "Stannum 30X", "labeler_name": "Uriel Pharmacy Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Stannum 30X", "active_ingredients": [{"name": "TIN", "strength": "30 [hp_X]/mL"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20090901", "listing_expiration_date": "20261231"}