Glucose and Sodium Chloride
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
- Glucose and Sodium Chloride
- Generic name
- DEXTROSE ANHYDROUS AND SODIUM CHLORIDE
- Manufacturer
- Baxter Healthcare Corporation
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 1ba918d0-13d0-48bc-8742-658fc0eb47b6
- SPL ID
- bf7a8e49-ae3a-484a-8437-d8dd72faba49
- Version
- 3
- Effective date
- 2025-01-24
- Source export date
- 2026-10-30
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/0b630a6825fc0c8abba22d7c8fd4d069bde78bef928766047ddbb369119f337f/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 18:57:53
| Harmonized routes |
|---|
| INTRAVENOUS |
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 |
|---|---|---|---|
| brand name | Glucose and Sodium Chloride | openfda.brand_name | |
| generic name | DEXTROSE ANHYDROUS AND SODIUM CHLORIDE | openfda.generic_name | |
| manufacturer name | Baxter Healthcare Corporation | openfda.manufacturer_name | |
| ndc | package | 0338-9799-01 | openfda.package_ndc |
| ndc | package | 0338-9799-12 | openfda.package_ndc |
| ndc | product | 0338-9799 | openfda.product_ndc |
| ndc11 | package | 00338979912 | derived:openfda.package_ndc |
| ndc11 | package | 00338979901 | derived:openfda.package_ndc |
| rxcui | 2698222 | openfda.rxcui | |
| spl id | bf7a8e49-ae3a-484a-8437-d8dd72faba49 | id | |
| spl set id | 1ba918d0-13d0-48bc-8742-658fc0eb47b6 | set_id | |
| unii | 451W47IQ8X | openfda.unii | |
| unii | LX22YL083G | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.