Sodium Chloride
- Product NDC
- 76420-083
- 11-digit product format
- 764200083
- Labeler code
- 76420
- Product ID
- 76420-083_b8e8faa1-b133-450e-e053-2995a90aeace
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Chloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
- Labeler
- Asclemed USA, Inc.
- Application
- NDA018803
- Marketing category
- NDA
- Marketing start
- 2005-02-28
- Substance
- SODIUM CHLORIDE
- Active strength
- 9 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sodium Chloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM CHLORIDE | 9 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 451W47IQ8X |
| Rxcui | 1807637 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 76420-083-10 | Sodium Chloride | 10 mL in 1 VIAL, SINGLE-DOSE | INJECTION, SOLUTION | 10 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76420-083 | SODIUM CHLORIDE INJECTION, SOLUTION [ASCLEMED USA, INC.] | 2 | Current NDC, Legacy NDC, 1 package rows | 20210116_a411c118-ef0e-4c42-9924-4a06ec690e94.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 76420-083-10 | 76420008310 | 10 mL in 1 VIAL, SINGLE-DOSE (76420-083-10) | 10 ml | 2020-04-09 | 0000-00-00 | No | No | Current |