Sodium Chloride
- Product NDC
- 50090-2488
- 11-digit product format
- 500902488
- Labeler code
- 50090
- Product ID
- 50090-2488_c864438f-bd15-4213-92fe-c1e9c8314703
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SODIUM CHLORIDE
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- A-S Medication Solutions
- Application
- ANDA088912
- Marketing category
- ANDA
- Marketing start
- 2000-08-10
- Marketing end
- 0000-00-00
- Substance
- SODIUM CHLORIDE
- Active strength
- 9 mg/mL
- Pharmacologic classes
- Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-2488-0 | 50090248800 | 25 VIAL, SINGLE-DOSE in 1 TRAY (50090-2488-0) > 10 mL in 1 VIAL, SINGLE-DOSE | 2016-10-12 | 0000-00-00 | No | No | Current |