Sodium Chloride
- Product NDC
- 85766-059
- 11-digit product format
- 857660059
- Labeler code
- 85766
- Product ID
- 85766-059_502f0bde-75a5-adca-e063-6394a90a5f87
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Chloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Sportpharm LLC
- 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
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 | 9 g/1000mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 451W47IQ8X |
| Rxcui | 1807639 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 85766-059-00 | Sodium Chloride | 1000 mL in 1 BAG | INJECTION, SOLUTION | 1000 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 85766-059-00 | 85766005900 | 1000 mL in 1 BAG (85766-059-00) | 1000 ml | 2025-08-22 | No | No | Current |