SODIUM CHLORIDE
- Product NDC
- 51662-1318
- 11-digit product format
- 516621318
- Labeler code
- 51662
- Product ID
- 51662-1318_9f23308a-6c72-23df-e053-2995a90aefe8
- 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
- 2018-11-26
- Marketing end
- 0000-00-00
- Substance
- SODIUM CHLORIDE
- Active strength
- 900 mg/100mL
- Pharmacologic classes
- Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51662-1318-1 | SODIUM CHLORIDE | 100 mL in 1 BAG | INJECTION, SOLUTION | 100 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51662-1318 | SODIUM CHLORIDE INJECTION, SOLUTION [HF ACQUISITION CO LLC, DBA HEALTHFIRST] | 3 | Legacy NDC, 1 package rows | 20200222_7b9820ba-1a2f-8b3f-e053-2991aa0abf64.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 |
|---|
| 51662-1318-1 | 51662131801 | 100 mL in 1 BAG (51662-1318-1) | 100 ml | 2018-11-26 | 0000-00-00 | No | No | Current |