FDA.reportPublic FDA data

Nitrogen

Manufacturer
WELDERS SUPPLY COMPANY OF LOUISVILLE, INC.
Effective date
2026-04-28
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-05-31 22:17:05

Label at a glance#

ProductNitrogen
Active ingredientNITROGEN
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NITROGEN, COMPRESSED NF

UN1066

Rx only. WARNING: Administration of Nitrogen may be hazardous or contraindicated. For use only by or under the supervision of a licensed practitioner who is experienced in the use and administration of Nitrogen and is familiar with the indications, effects, dosages, methods, and frequency and duration of administration, and with the hazards, contraindications and side effects, and the precautions to be taken. WARNING: CONTAINS GAS UNDER PRESSURE; MAY EXPLODE IF HEATED. MAY DISPLACE OXYGEN AND CAUSE RAPID SUFFOCATION. Do not handle until all safety precautions have been read and understood. Use and store only outdoors or in a well-ventilated place. Use a back flow preventive device in the piping. Use only with equipment rated for cylinder pressure. Close valve after each use and when empty. Protect from sunlight when ambient temperature exceeds 52 C (125 F). Read and follow the Safety Data Sheet (SDS) before use. FIRST AID: IF INHALED: Remove person to fresh air and keep comfortable for breathing. Get medical advice/attention. CAS: 7727-37-9

CONTENTS: LTRS: CU.FT.

WELDERS SUPPLY & GASES

331 Boxley Avenue. Louisville, KY 40209

502-637-4771 nitrogennitrogen

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
348624nitrogen 99.2 % Gas for InhalationPSN7
348624nitrogen 99.2 % Gas for InhalationSCD7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84078-001-01Nitrogen8501 L in 1 CYLINDERGAS85017
84078-001-02Nitrogen230 L in 1 CYLINDERGAS2307
84078-001-03Nitrogen6453 L in 1 CYLINDERGAS64537
84078-001-04Nitrogen651 L in 1 CYLINDERGAS6517
84078-001-05Nitrogen1090 L in 1 CYLINDERGAS10907
84078-001-06Nitrogen5924 L in 1 CYLINDERGAS59247
84078-001-07Nitrogen7810 L in 1 CYLINDERGAS78107
84078-001-08Nitrogen104300 L in 1 CYLINDERGAS1043007
84078-001-09Nitrogen116100 L in 1 CYLINDERGAS1161007
84078-001-10Nitrogen230 L in 1 CYLINDERGAS2307
84078-001-11Nitrogen160 L in 1 CYLINDERGAS1607
84078-001-12Nitrogen180 L in 1 CYLINDERGAS1807

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 1 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84078-00184078-001-01, 84078-001-02, 84078-001-03, 84078-001-04, 84078-001-05, 84078-001-06, 84078-001-07, 84078-001-08, 84078-001-09, 84078-001-10, 84078-001-11, 84078-001-12

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
NameUNIIKind
NITROGENN762921K75ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
52026-01-28monthly-update2026-06-03 17:55:44
42025-12-30monthly-update2026-06-03 17:49:17

Orange Book application contexts#

All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.

Orange Book application contexts page 1 of 1 · 1 matching rows.

Source provenance: Browse the complete Orange Book source catalog.

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
NitrogenNITROGENWELDERS SUPPLY COMPANY OF LOUISVILLE, INC.1017e562-498d-9554-e063-6394a90ab5662026-04-28Exact identifier
ndc (package): 84078-001-12
ndc (package): 84078-001-11
ndc (package): 84078-001-08
ndc (package): 84078-001-06
ndc (package): 84078-001-03
ndc (package): 84078-001-04
ndc (package): 84078-001-02
ndc (package): 84078-001-01
ndc (package): 84078-001-07
ndc (package): 84078-001-09
ndc (package): 84078-001-10
ndc (package): 84078-001-05
ndc (product): 84078-001
ndc11 (package): 84078000105
ndc11 (package): 84078000112
ndc11 (package): 84078000103
ndc11 (package): 84078000109
ndc11 (package): 84078000106
ndc11 (package): 84078000108
ndc11 (package): 84078000104
ndc11 (package): 84078000110
ndc11 (package): 84078000101
ndc11 (package): 84078000102
ndc11 (package): 84078000111
ndc11 (package): 84078000107
spl id: 50871b9d-735b-0673-e063-6294a90a560d
spl set id: 1017e562-498d-9554-e063-6394a90ab566

Reported adverse events (FAERS/openFDA)#

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