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
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 |
|---|
| 76420-083-10 | 76420008310 | 10 mL in 1 VIAL, SINGLE-DOSE (76420-083-10) | 10 ml | 2020-04-09 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| 0.9% Sodium Chloride | Asclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM | 2021-01-14 | HUMAN PRESCRIPTION DRUG LABEL | 2 |