Lactated Ringers
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
- Lactated Ringers
- Generic name
- SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE
- Manufacturer
- Baxter Healthcare Corporation
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- f09f80bf-2f8b-4420-865d-aec2d5e5cd4d
- SPL ID
- 890d485f-ede2-4141-8672-2edbeb9639a4
- Version
- 10
- Effective date
- 2012-06-12
- Source export date
- 2026-10-30
- Source partition
- 10
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/3b4c9bc1c064560160661a043b9878894ba805e5e90f4733fb76824b6ba7ac42/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 19:20:20
| Harmonized routes |
|---|
| IRRIGATION |
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 | 018494 | derived:openfda.application_number |
| application number | NDA018494 | openfda.application_number | |
| brand name | Lactated Ringers | openfda.brand_name | |
| generic name | SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE | openfda.generic_name | |
| manufacturer name | Baxter Healthcare Corporation | openfda.manufacturer_name | |
| ndc | package | 0338-0114-04 | openfda.package_ndc |
| ndc | product | 0338-0114 | openfda.product_ndc |
| ndc11 | package | 00338011404 | derived:openfda.package_ndc |
| rxcui | 847628 | openfda.rxcui | |
| spl id | 890d485f-ede2-4141-8672-2edbeb9639a4 | id | |
| spl set id | f09f80bf-2f8b-4420-865d-aec2d5e5cd4d | set_id | |
| unii | TU7HW0W0QT | openfda.unii | |
| unii | 451W47IQ8X | openfda.unii | |
| unii | 660YQ98I10 | openfda.unii | |
| unii | M4I0D6VV5M | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.