SODIUM CHLORIDE
- Product NDC
- 0338-9660
- 11-digit product format
- 003389660
- Labeler code
- 0338
- Product ID
- 0338-9660_8b17d4cf-858a-40e5-bcdd-23e3d9b80180
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- sodium chloride
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Baxter Healthcare Corporation
- Application
- NDA020178
- Marketing category
- NDA
- Marketing start
- 1992-12-07
- Substance
- SODIUM CHLORIDE
- Active strength
- 450 mg/50mL
- Pharmacologic classes
- Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0338-9660-40 | SODIUM CHLORIDE | 40 in 1 CARTON | INJECTION | 40 | | 3 |
| 0338-9660-40 | SODIUM CHLORIDE | 50 mL in 1 BAG | INJECTION | 50 | | 3 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 0338-9660-40 | 00338966040 | 40 BAG in 1 CARTON (0338-9660-40) / 50 mL in 1 BAG | 40 bag | 2025-07-30 | No | No | Historical |