Liquid Nitrogen NF

Manufacturer: Linde Inc. | Linde Inc
Effective date: 2026-07-16
Label type: HUMAN PRESCRIPTION DRUG LABEL
Version: 33
Source: daily-update
Hydrated at: 2026-07-21 05:10:30

Label at a glance#

ProductNitrogen

Active ingredientNITROGEN

Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Proof of Delivery

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version	Uploaded
nitrogen	ACTIVE INGREDIENT	N762921K75	1
NITROGEN	ACTIVE MOIETY	N762921K75	1

Products#

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

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

Nitrogen

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
59578-499	59578-499-01

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
Name	UNII	Kind
NITROGEN	N762921K75	ACTIB

Source Document#

Source XML · Source PDF

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
32	2025-12-30	full-release	2026-05-31 21:53:05

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Nitrogen	NITROGEN	Linde Inc.	11f1ea16-93eb-4994-ba96-d0d7519015e2	2026-07-16		Exact identifier ndc (package): 59578-499-01 ndc (product): 59578-499 ndc11 (package): 59578049901 spl id: 56bc9edc-dafc-b316-e063-6394a90aa5e7 spl set id: 11f1ea16-93eb-4994-ba96-d0d7519015e2

Reported adverse events (FAERS/openFDA)#

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