Package 48951-8361-1

Brand: stannum 21x

Generic: stannum 21x
NDC Package

Package Facts

Identity

Package NDC 48951-8361-1
Digits Only 4895183611
Product NDC 48951-8361
Product ID 48951-8361_4886865e-c543-7b22-e063-6394a90a6f14
Description

10 AMPULE in 1 BOX (48951-8361-1) / 1 mL in 1 AMPULE

Marketing

Marketing Status
Marketed Since 2009-09-01
Brand stannum 21x
Generic stannum 21x
Sample Package No

Linked Drug Pages (1)

Stannum 21X ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4886865e-c543-7b22-e063-6394a90a6f14", "openfda": {"unii": ["387GMG9FH5"], "spl_set_id": ["969cb4b7-c1c2-0577-e053-2a95a90a4e2c"], "manufacturer_name": ["Uriel Pharmacy Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 AMPULE in 1 BOX (48951-8361-1)  / 1 mL in 1 AMPULE", "package_ndc": "48951-8361-1", "marketing_start_date": "20090901"}], "brand_name": "Stannum 21X", "product_id": "48951-8361_4886865e-c543-7b22-e063-6394a90a6f14", "dosage_form": "LIQUID", "product_ndc": "48951-8361", "generic_name": "Stannum 21X", "labeler_name": "Uriel Pharmacy Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Stannum 21X", "active_ingredients": [{"name": "TIN", "strength": "21 [hp_X]/mL"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20090901", "listing_expiration_date": "20271231"}