Sodium Chloride
- Product NDC
- 52584-888
- 11-digit product format
- 525840888
- Labeler code
- 52584
- Product ID
- 52584-888_d1e5787a-3258-4229-92b5-84cc35012a78
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Chloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
- Labeler
- General Injectables & Vaccines, Inc
- Application
- NDA018803
- Marketing category
- NDA
- Marketing start
- 2010-08-01
- Marketing end
- 0000-00-00
- Substance
- SODIUM CHLORIDE
- Active strength
- 9 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 52584-888-20 | 52584088820 | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-888-20) > 20 mL in 1 VIAL, SINGLE-DOSE | 2016-09-14 | 0000-00-00 | No | No | Current |
| 52584-888-50 | 52584088850 | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-888-50) > 50 mL in 1 VIAL, SINGLE-DOSE | 2016-09-14 | 0000-00-00 | No | No | Current |