SODIUM CHLORIDE
- Product NDC
- 0338-9661
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- sodium chloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Baxter Healthcare Corporation
- Application
- NDA016677
- Marketing category
- NDA
- Substance
- SODIUM CHLORIDE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 0338-9661-60 | 100 mL in 1 BAG (0338-9661-60) | 2024-08-09 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Sodium Chloride Injection, USP in VIAFLO Plastic Container | Baxter Healthcare Corporation | Bieffe Medital SA | 2024-08-09 | HUMAN PRESCRIPTION DRUG LABEL | 19 |