Sodium Chloride
- Product NDC
- 84549-888
- 11-digit product format
- 845490888
- Labeler code
- 84549
- Product ID
- 84549-888_48d73434-e65c-dc98-e063-6294a90affa2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Chloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
- Labeler
- ProPharma Distribution
- 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
- 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 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 |
|---|
| 84549-888-10 | Sodium Chloride | 10 mL in 1 VIAL, SINGLE-DOSE | INJECTION, SOLUTION | 10 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84549-888-10 | 84549088810 | 10 mL in 1 VIAL, SINGLE-DOSE (84549-888-10) | 10 ml | 2026-01-20 | No | No | Historical |