iopamidol
Generic: iopamidol
Labeler: slate run pharmaceuticalsDrug Facts
Product Profile
Brand Name
iopamidol
Generic Name
iopamidol
Labeler
slate run pharmaceuticals
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
iopamidol 612 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
70436-126
Product ID
70436-126_16308b6e-8a2e-8431-e063-6294a90a986c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA215382
Listing Expiration
2026-12-31
Marketing Start
2023-07-20
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
70436126
Hyphenated Format
70436-126
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
iopamidol (source: ndc)
Generic Name
iopamidol (source: ndc)
Application Number
ANDA215382 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 612 mg/mL
Packaging
- 15 mL in 1 VIAL, SINGLE-DOSE (70436-126-34)
- 150 mL in 1 CARTON (70436-126-82)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRATHECAL"], "spl_id": "16308b6e-8a2e-8431-e063-6294a90a986c", "openfda": {"nui": ["N0000180185", "N0000010258"], "unii": ["JR13W81H44"], "spl_set_id": ["0b9e0d24-c6ca-4e22-9422-936e9d475eaa"], "pharm_class_epc": ["Radiographic Contrast Agent [EPC]"], "pharm_class_moa": ["X-Ray Contrast Activity [MoA]"], "manufacturer_name": ["Slate Run Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "15 mL in 1 VIAL, SINGLE-DOSE (70436-126-34)", "package_ndc": "70436-126-34", "marketing_start_date": "20230720"}, {"sample": false, "description": "150 mL in 1 CARTON (70436-126-82)", "package_ndc": "70436-126-82", "marketing_start_date": "20230720"}], "brand_name": "iopamidol", "product_id": "70436-126_16308b6e-8a2e-8431-e063-6294a90a986c", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Radiographic Contrast Agent [EPC]", "X-Ray Contrast Activity [MoA]"], "product_ndc": "70436-126", "generic_name": "iopamidol", "labeler_name": "Slate Run Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "iopamidol", "active_ingredients": [{"name": "IOPAMIDOL", "strength": "612 mg/mL"}], "application_number": "ANDA215382", "marketing_category": "ANDA", "marketing_start_date": "20230720", "listing_expiration_date": "20261231"}