SODIUM CHLORIDE
- Product NDC
- 0338-9663
- 11-digit product format
- 003389663
- Labeler code
- 0338
- Product ID
- 0338-9663_ba9e58a5-60c5-4aab-9cef-36320d052091
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- sodium chloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Baxter Healthcare Corporation
- Application
- NDA016677
- Marketing category
- NDA
- Marketing start
- 1970-12-09
- Substance
- SODIUM CHLORIDE
- Active strength
- 9 g/1000mL
- 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 451W47IQ8X | SODIUM CHLORIDE | 7647-14-5 | SODIUM CHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 0338-9663-60 | 00338966360 | 100 mL in 1 BAG (0338-9663-60) | 100 ml | 2024-08-09 | No | No | Historical |