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
- HARTMAN BROTHERS, INC.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 123ca615-78ce-4bc8-bcae-168c4740c230
- SPL ID
- 41edf7a5-0356-fb6b-e063-6394a90a98cc
- Version
- 14
- 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 | 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 | HARTMAN BROTHERS, INC. | openfda.manufacturer_name | |
| ndc | package | 49204-002-19 | openfda.package_ndc |
| ndc | package | 49204-002-15 | openfda.package_ndc |
| ndc | package | 49204-002-06 | openfda.package_ndc |
| ndc | package | 49204-002-21 | openfda.package_ndc |
| ndc | package | 49204-002-08 | openfda.package_ndc |
| ndc | package | 49204-002-18 | openfda.package_ndc |
| ndc | package | 49204-002-22 | openfda.package_ndc |
| ndc | package | 49204-002-20 | openfda.package_ndc |
| ndc | package | 49204-002-13 | openfda.package_ndc |
| ndc | package | 49204-002-14 | openfda.package_ndc |
| ndc | package | 49204-002-10 | openfda.package_ndc |
| ndc | package | 49204-002-24 | openfda.package_ndc |
| ndc | package | 49204-002-16 | openfda.package_ndc |
| ndc | package | 49204-002-17 | openfda.package_ndc |
| ndc | package | 49204-002-07 | openfda.package_ndc |
| ndc | package | 49204-002-09 | openfda.package_ndc |
| ndc | package | 49204-002-23 | openfda.package_ndc |
| ndc | package | 49204-002-11 | openfda.package_ndc |
| ndc | package | 49204-002-12 | openfda.package_ndc |
| ndc | product | 49204-002 | openfda.product_ndc |
| ndc11 | package | 49204000213 | derived:openfda.package_ndc |
| ndc11 | package | 49204000217 | derived:openfda.package_ndc |
| ndc11 | package | 49204000209 | derived:openfda.package_ndc |
| ndc11 | package | 49204000218 | derived:openfda.package_ndc |
| ndc11 | package | 49204000208 | derived:openfda.package_ndc |
| ndc11 | package | 49204000216 | derived:openfda.package_ndc |
| ndc11 | package | 49204000211 | derived:openfda.package_ndc |
| ndc11 | package | 49204000222 | derived:openfda.package_ndc |
| ndc11 | package | 49204000215 | derived:openfda.package_ndc |
| ndc11 | package | 49204000206 | derived:openfda.package_ndc |
| ndc11 | package | 49204000223 | derived:openfda.package_ndc |
| ndc11 | package | 49204000220 | derived:openfda.package_ndc |
| ndc11 | package | 49204000212 | derived:openfda.package_ndc |
| ndc11 | package | 49204000219 | derived:openfda.package_ndc |
| ndc11 | package | 49204000214 | derived:openfda.package_ndc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.