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
- Arcet Equipment Company dba Arc3 Gases North
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- ff2ba9fb-e58a-4e57-8e96-b7e90cc6e2a8
- SPL ID
- 548b96ce-adbc-4cca-e063-6394a90a9411
- Version
- 17
- Effective date
- 2026-06-18
- Source export date
- 2026-10-30
- Source partition
- 14
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/7f38ccf216257b076837276c278194f298b4ccda641215a8f83814b33a860b51/drug-label-0014-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 20:00:56
| 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 | 205713 | derived:openfda.application_number |
| application number | NDA205713 | openfda.application_number | |
| brand name | Nitrogen | openfda.brand_name | |
| generic name | NITROGEN | openfda.generic_name | |
| manufacturer name | Arcet Equipment Company dba Arc3 Gases North | openfda.manufacturer_name | |
| ndc | package | 59788-002-12 | openfda.package_ndc |
| ndc | package | 59788-002-18 | openfda.package_ndc |
| ndc | package | 59788-002-20 | openfda.package_ndc |
| ndc | package | 59788-002-21 | openfda.package_ndc |
| ndc | package | 59788-002-17 | openfda.package_ndc |
| ndc | package | 59788-002-23 | openfda.package_ndc |
| ndc | package | 59788-002-24 | openfda.package_ndc |
| ndc | package | 59788-002-14 | openfda.package_ndc |
| ndc | package | 59788-002-13 | openfda.package_ndc |
| ndc | package | 59788-002-22 | openfda.package_ndc |
| ndc | package | 59788-002-10 | openfda.package_ndc |
| ndc | package | 59788-002-19 | openfda.package_ndc |
| ndc | package | 59788-002-09 | openfda.package_ndc |
| ndc | package | 59788-002-15 | openfda.package_ndc |
| ndc | package | 59788-002-11 | openfda.package_ndc |
| ndc | package | 59788-002-16 | openfda.package_ndc |
| ndc | product | 59788-002 | openfda.product_ndc |
| ndc11 | package | 59788000218 | derived:openfda.package_ndc |
| ndc11 | package | 59788000212 | derived:openfda.package_ndc |
| ndc11 | package | 59788000209 | derived:openfda.package_ndc |
| ndc11 | package | 59788000222 | derived:openfda.package_ndc |
| ndc11 | package | 59788000217 | derived:openfda.package_ndc |
| ndc11 | package | 59788000220 | derived:openfda.package_ndc |
| ndc11 | package | 59788000219 | derived:openfda.package_ndc |
| ndc11 | package | 59788000213 | derived:openfda.package_ndc |
| ndc11 | package | 59788000223 | derived:openfda.package_ndc |
| ndc11 | package | 59788000216 | derived:openfda.package_ndc |
| ndc11 | package | 59788000215 | derived:openfda.package_ndc |
| ndc11 | package | 59788000214 | derived:openfda.package_ndc |
| ndc11 | package | 59788000211 | derived:openfda.package_ndc |
| ndc11 | package | 59788000210 | derived:openfda.package_ndc |
| ndc11 | package | 59788000221 | derived:openfda.package_ndc |
| ndc11 | package | 59788000224 | derived:openfda.package_ndc |
| rxcui | 311998 | openfda.rxcui | |
| spl id | 548b96ce-adbc-4cca-e063-6394a90a9411 | id |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.