Sodium Chloride
- Product NDC
- 63323-139
- Requested package NDC
- 63323-139-40
- 11-digit product format
- 633230139
- Labeler code
- 63323
- Product ID
- 63323-139_946c3735-c530-46c5-e053-2a95a90ae5af
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SODIUM CHLORIDE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Fresenius Kabi USA, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2000-09-06
- Marketing end
- 0000-00-00
- Substance
- SODIUM CHLORIDE
- Active strength
- 146 mg/mL
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts#
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63323-139 | SODIUM CHLORIDE INJECTION, SOLUTION [FRESENIUS KABI USA, LLC] | 3 | Legacy NDC | 20241017_ef09b4e7-ccc5-41c8-ba66-beb7a56d2e67.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63323-139-40 | 63323013940 | 25 VIAL, SINGLE-DOSE in 1 TRAY (63323-139-40) > 40 mL in 1 VIAL, SINGLE-DOSE | 2000-09-06 | 0000-00-00 | No | No | Current |