Nitrogen
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
- Brand name
- Nitrogen
- Generic name
- NITROGEN
- Manufacturer
- DuPuy Oxygen & Supply Company, Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 6cf60077-dc91-41e5-8d6f-22589a66e6c5
- SPL ID
- 41eb9a2e-5872-24a4-e063-6294a90ac6ec
- Version
- 17
- Effective date
- 2025-10-24
- Source export date
- 2026-09-28
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:26:19
| Harmonized routes |
|---|
| RESPIRATORY (INHALATION) |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application applno | NDA | 205850 | derived:openfda.application_number |
| application number | NDA205850 | openfda.application_number | |
| brand name | Nitrogen | openfda.brand_name | |
| generic name | NITROGEN | openfda.generic_name | |
| manufacturer name | DuPuy Oxygen & Supply Company, Inc. | openfda.manufacturer_name | |
| ndc | package | 50554-002-09 | openfda.package_ndc |
| ndc | package | 50554-002-06 | openfda.package_ndc |
| ndc | package | 50554-002-08 | openfda.package_ndc |
| ndc | package | 50554-002-14 | openfda.package_ndc |
| ndc | package | 50554-002-07 | openfda.package_ndc |
| ndc | package | 50554-002-11 | openfda.package_ndc |
| ndc | package | 50554-002-10 | openfda.package_ndc |
| ndc | package | 50554-002-13 | openfda.package_ndc |
| ndc | package | 50554-002-12 | openfda.package_ndc |
| ndc | product | 50554-002 | openfda.product_ndc |
| ndc11 | package | 50554000207 | derived:openfda.package_ndc |
| ndc11 | package | 50554000214 | derived:openfda.package_ndc |
| ndc11 | package | 50554000211 | derived:openfda.package_ndc |
| ndc11 | package | 50554000208 | derived:openfda.package_ndc |
| ndc11 | package | 50554000210 | derived:openfda.package_ndc |
| ndc11 | package | 50554000212 | derived:openfda.package_ndc |
| ndc11 | package | 50554000213 | derived:openfda.package_ndc |
| ndc11 | package | 50554000206 | derived:openfda.package_ndc |
| ndc11 | package | 50554000209 | derived:openfda.package_ndc |
| rxcui | 311998 | openfda.rxcui | |
| spl id | 41eb9a2e-5872-24a4-e063-6294a90ac6ec | id | |
| spl set id | 6cf60077-dc91-41e5-8d6f-22589a66e6c5 | set_id | |
| unii | N762921K75 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.