Ammonia N 13

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Ammonia N 13
Generic name: AMMONIA N-13
Manufacturer: Kreitchman PET Center
Product type: HUMAN PRESCRIPTION DRUG
SPL set ID: 26572b37-0999-4c83-8206-1c088026d407
SPL ID: bf01478c-3377-4b2c-905c-30807e865825
Version: 7
Effective date: 2026-01-27
Source export date: 2026-10-12
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:43:23

Harmonized routes table
Harmonized routes
INTRAVENOUS

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application applno	ANDA	203938	derived:openfda.application_number
application number		ANDA203938	openfda.application_number
brand name		Ammonia N 13	openfda.brand_name
generic name		AMMONIA N-13	openfda.generic_name
manufacturer name		Kreitchman PET Center	openfda.manufacturer_name
ndc	package	62072-456-56	openfda.package_ndc
ndc	product	62072-456	openfda.product_ndc
ndc11	package	62072045656	derived:openfda.package_ndc
spl id		bf01478c-3377-4b2c-905c-30807e865825	id
spl set id		26572b37-0999-4c83-8206-1c088026d407	set_id
unii		9OQO0E343Z	openfda.unii

Adverse reactions cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Adverse reactions sections page 1 of 1 · 1 matching rows.

adverse reactions

6 ADVERSE REACTIONS No adverse reactions have been reported for Ammonia N 13 Injection based on a review of the published literature, publicly available reference sources, and adverse drug reaction reporting systems. However, the completeness of these sources is not known. No adverse reactions have been reported for Ammonia N 13 Injection based on a review of the published literature, publicly available reference sources, and adverse drug reaction reporting system (6) . To report SUSPECTED ADVERSE REACTIONS, contact Kreitchman PET Center at 212-305-0081 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.