SODIUM CHLORIDE
- Product NDC
- 51662-1522
- 11-digit product format
- 516621522
- Labeler code
- 51662
- Product ID
- 51662-1522_ac0fd44a-3f3a-8d7e-e053-2995a90afeec
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SODIUM CHLORIDE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- HF Acquisition Co LLC, DBA HealthFirst
- Application
- NDA016366
- Marketing category
- NDA
- Marketing start
- 2020-08-04
- Substance
- SODIUM CHLORIDE
- Active strength
- 900 mg/100mL
- 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 | 900 mg/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 451W47IQ8X |
| Rxcui | 1807634 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51662-1522-1 | SODIUM CHLORIDE | 500 mL in 1 BAG | INJECTION, SOLUTION | 500 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51662-1522 | SODIUM CHLORIDE INJECTION, SOLUTION [HF ACQUISITION CO LLC, DBA HEALTHFIRST] | 1 | Current NDC, Legacy NDC, 1 package rows | 20200805_ac0fd44a-3f39-8d7e-e053-2995a90afeec.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 |
|---|
| 51662-1522-1 | 51662152201 | 500 mL in 1 BAG (51662-1522-1) | 500 ml | 2020-08-04 | 0000-00-00 | No | No | Current |