Sodium Chloride
- Product NDC
- 0409-7985
- 11-digit product format
- 004097985
- Labeler code
- 0409
- Product ID
- 0409-7985_9788db74-ff4f-41d6-9c2e-f8d4850e5662
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SODIUM CHLORIDE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Hospira, Inc.
- Application
- NDA018090
- Marketing category
- NDA
- Marketing start
- 1979-04-04
- Marketing end
- 2022-07-08
- Substance
- SODIUM CHLORIDE
- Active strength
- 450 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0409-7985-03 | 00409798503 | 24 POUCH in 1 CASE (0409-7985-03) > 1 BAG in 1 POUCH > 500 mL in 1 BAG | 24 pouch | 1979-04-04 | 2022-07-08 | No | No | Current |
| 0409-7985-09 | 00409798509 | 12 POUCH in 1 CASE (0409-7985-09) > 1 BAG in 1 POUCH > 1000 mL in 1 BAG | 12 pouch | 1979-04-04 | 2022-07-08 | No | No | Current |