0.9% SODIUM CHLORIDE
- Product NDC
- 51662-1609
- 11-digit product format
- 516621609
- Labeler code
- 51662
- Product ID
- 51662-1609_0ffa8cc4-f3fa-0814-e063-6294a90a9234
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- 0.9% SODIUM CHLORIDE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- HF Acquisition Co LLC, DBA HealthFirst
- Application
- ANDA207956
- Marketing category
- ANDA
- Marketing start
- 2022-07-31
- Substance
- SODIUM CHLORIDE
- Active strength
- 9 g/1000mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- 0.9% SODIUM CHLORIDE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM CHLORIDE | 9 g/1000mL |
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 |
|---|
| 51662-1609-1 | 0.9% SODIUM CHLORIDE | 500 mL in 1 BAG | INJECTION, SOLUTION | 500 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51662-1609 | 0.9% SODIUM CHLORIDE INJECTION, SOLUTION [HF ACQUISITION CO LLC, DBA HEALTHFIRST] | 2 | Current NDC, Legacy NDC, 1 package rows | 20240129_e5247ed5-6170-c13f-e053-2a95a90a4101.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 |
|---|
| 51662-1609-1 | 51662160901 | 500 mL in 1 BAG (51662-1609-1) | 500 ml | 2022-07-31 | 0000-00-00 | No | No | Current |