ammonia n 13
Generic: ammonia n-13
Labeler: ionetix corporationDrug Facts
Product Profile
Brand Name
ammonia n 13
Generic Name
ammonia n-13
Labeler
ionetix corporation
Dosage Form
INJECTION
Routes
Active Ingredients
ammonia n-13 37.5 mCi/mL
Manufacturer
Identifiers & Regulatory
Product NDC
71162-001
Product ID
71162-001_36b0308e-2204-31d0-e063-6394a90a4578
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210524
Listing Expiration
2026-12-31
Marketing Start
2018-12-21
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71162001
Hyphenated Format
71162-001
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
ammonia n 13 (source: ndc)
Generic Name
ammonia n-13 (source: ndc)
Application Number
ANDA210524 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 37.5 mCi/mL
Packaging
- 5 mL in 1 SYRINGE, PLASTIC (71162-001-05)
- 1 VIAL, GLASS in 1 CONTAINER (71162-001-10) / 10 mL in 1 VIAL, GLASS
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "36b0308e-2204-31d0-e063-6394a90a4578", "openfda": {"nui": ["N0000177914", "N0000000205"], "unii": ["9OQO0E343Z"], "spl_set_id": ["61e196ba-3812-4ffd-8032-12b215378fef"], "pharm_class_epc": ["Radioactive Diagnostic Agent [EPC]"], "pharm_class_moa": ["Radiopharmaceutical Activity [MoA]"], "manufacturer_name": ["Ionetix Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 mL in 1 SYRINGE, PLASTIC (71162-001-05)", "package_ndc": "71162-001-05", "marketing_start_date": "20200131"}, {"sample": false, "description": "1 VIAL, GLASS in 1 CONTAINER (71162-001-10) / 10 mL in 1 VIAL, GLASS", "package_ndc": "71162-001-10", "marketing_start_date": "20181221"}], "brand_name": "Ammonia N 13", "product_id": "71162-001_36b0308e-2204-31d0-e063-6394a90a4578", "dosage_form": "INJECTION", "pharm_class": ["Radioactive Diagnostic Agent [EPC]", "Radiopharmaceutical Activity [MoA]"], "product_ndc": "71162-001", "generic_name": "Ammonia N-13", "labeler_name": "Ionetix Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ammonia N 13", "active_ingredients": [{"name": "AMMONIA N-13", "strength": "37.5 mCi/mL"}], "application_number": "ANDA210524", "marketing_category": "ANDA", "marketing_start_date": "20181221", "listing_expiration_date": "20261231"}