e-z-disk
Generic: barium sulfate
Labeler: e-z-em, inc.Drug Facts
Product Profile
Brand Name
e-z-disk
Generic Name
barium sulfate
Labeler
e-z-em, inc.
Dosage Form
TABLET
Routes
Active Ingredients
barium sulfate 700 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
10361-778
Product ID
10361-778_29014e07-78d9-38c1-1945-8cb44ec6f69b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA219840
Listing Expiration
2026-12-31
Marketing Start
2009-02-01
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
10361778
Hyphenated Format
10361-778
Supplemental Identifiers
UNII
NUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
e-z-disk (source: ndc)
Generic Name
barium sulfate (source: ndc)
Application Number
NDA219840 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 700 mg/1
Packaging
- 100 TABLET in 1 BOTTLE, GLASS (10361-778-31)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "29014e07-78d9-38c1-1945-8cb44ec6f69b", "openfda": {"nui": ["N0000180185", "N0000010258"], "unii": ["25BB7EKE2E"], "spl_set_id": ["c759668b-5cf1-b237-00c8-a5e4733b6f4c"], "pharm_class_epc": ["Radiographic Contrast Agent [EPC]"], "pharm_class_moa": ["X-Ray Contrast Activity [MoA]"], "manufacturer_name": ["E-Z-EM, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, GLASS (10361-778-31)", "package_ndc": "10361-778-31", "marketing_start_date": "20090201"}], "brand_name": "E-Z-Disk", "product_id": "10361-778_29014e07-78d9-38c1-1945-8cb44ec6f69b", "dosage_form": "TABLET", "pharm_class": ["Radiographic Contrast Agent [EPC]", "X-Ray Contrast Activity [MoA]"], "product_ndc": "10361-778", "generic_name": "barium sulfate", "labeler_name": "E-Z-EM, INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "E-Z-Disk", "active_ingredients": [{"name": "BARIUM SULFATE", "strength": "700 mg/1"}], "application_number": "NDA219840", "marketing_category": "NDA", "marketing_start_date": "20090201", "listing_expiration_date": "20261231"}