SODIUM CHLORIDE
- Product NDC
- 0338-9662
- 11-digit product format
- 003389662
- Labeler code
- 0338
- Product ID
- 0338-9662_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
- 900 mg/100mL
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- SODIUM CHLORIDE
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM CHLORIDE | 900 mg/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 451W47IQ8X |
| Rxcui | 1807631, 1807632 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0338-9662-35 | SODIUM CHLORIDE | 35 in 1 CARTON | INJECTION | 35 | | 3 |
| 0338-9662-35 | SODIUM CHLORIDE | 100 mL in 1 BAG | INJECTION | 100 | | 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 |
|---|
| 0338-9662-35 | 00338966235 | 35 BAG in 1 CARTON (0338-9662-35) / 100 mL in 1 BAG | 35 bag | 2025-07-30 | No | No | Historical |