Nitrogen
- Manufacturer
- Linde Canada Inc. | Linde Canada, Inc.
- Effective date
- 2025-12-30
- Label type
- HUMAN PRESCRIPTION DRUG LABEL
- Version
- 24
- Source
- full-release
- Hydrated at
- 2026-05-31 21:53:21
Label at a glance#
ProductNitrogen
Active ingredientNITROGEN
Label structure1 sections
Label contents#
Full prescribing information#
DailyMed RxNorm Mappings#
Product Linked Resources#
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Data code | Code 39 | 24212885 | LindeCanPoDNFN2.jpg |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 49479-500-01 | Nitrogen | 26000 L in 1 TANK | GAS | 26000 | 24 |
DailyMed Socrata Ingredients#
| 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.
- Nitrogen
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 49479-500 | 49479-500-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| NITROGEN | N762921K75 | ACTIB |
Source Document#
Orange Book application contexts#
All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Nitrogen | NITROGEN | Linde Canada Inc. | 7fd42cc1-8e1e-43b3-981b-d0d6cf454f5a | 2025-12-30 | 49479-500-01 49479-500 49479050001 47319980-dc78-c214-e063-6294a90ac06f 7fd42cc1-8e1e-43b3-981b-d0d6cf454f5a |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
