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
- ANALGESIC SERVICES, INC.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- c15972b6-24af-4f5a-a244-7c155d5cc4a9
- SPL ID
- 42518a2d-050b-f3c8-e063-6394a90a52e1
- Version
- 14
- Effective date
- 2025-10-29
- Source export date
- 2026-10-12
- 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/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:54:34
| 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 | ANALGESIC SERVICES, INC. | openfda.manufacturer_name | |
| ndc | package | 52085-002-07 | openfda.package_ndc |
| ndc | package | 52085-002-05 | openfda.package_ndc |
| ndc | package | 52085-002-09 | openfda.package_ndc |
| ndc | package | 52085-002-08 | openfda.package_ndc |
| ndc | package | 52085-002-15 | openfda.package_ndc |
| ndc | package | 52085-002-14 | openfda.package_ndc |
| ndc | package | 52085-002-01 | openfda.package_ndc |
| ndc | package | 52085-002-04 | openfda.package_ndc |
| ndc | package | 52085-002-06 | openfda.package_ndc |
| ndc | package | 52085-002-03 | openfda.package_ndc |
| ndc | package | 52085-002-02 | openfda.package_ndc |
| ndc | package | 52085-002-13 | openfda.package_ndc |
| ndc | package | 52085-002-10 | openfda.package_ndc |
| ndc | package | 52085-002-12 | openfda.package_ndc |
| ndc | package | 52085-002-11 | openfda.package_ndc |
| ndc | product | 52085-002 | openfda.product_ndc |
| ndc11 | package | 52085000215 | derived:openfda.package_ndc |
| ndc11 | package | 52085000202 | derived:openfda.package_ndc |
| ndc11 | package | 52085000209 | derived:openfda.package_ndc |
| ndc11 | package | 52085000204 | derived:openfda.package_ndc |
| ndc11 | package | 52085000205 | derived:openfda.package_ndc |
| ndc11 | package | 52085000201 | derived:openfda.package_ndc |
| ndc11 | package | 52085000208 | derived:openfda.package_ndc |
| ndc11 | package | 52085000211 | derived:openfda.package_ndc |
| ndc11 | package | 52085000213 | derived:openfda.package_ndc |
| ndc11 | package | 52085000203 | derived:openfda.package_ndc |
| ndc11 | package | 52085000212 | derived:openfda.package_ndc |
| ndc11 | package | 52085000207 | derived:openfda.package_ndc |
| ndc11 | package | 52085000210 | derived:openfda.package_ndc |
| ndc11 | package | 52085000214 | derived:openfda.package_ndc |
| ndc11 | package | 52085000206 | derived:openfda.package_ndc |
| rxcui | 311998 | openfda.rxcui | |
| spl id | 42518a2d-050b-f3c8-e063-6394a90a52e1 | id | |
| spl set id | c15972b6-24af-4f5a-a244-7c155d5cc4a9 | set_id | |
| unii | N762921K75 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.