Dextrose and Sodium Chloride
- Product NDC
- 0409-7925
- 11-digit product format
- 004097925
- Labeler code
- 0409
- Product ID
- 0409-7925_62889680-51df-4213-9667-4f3433523499
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DEXTROSE MONOHYDRATE and SODIUM CHLORIDE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Hospira, Inc.
- Application
- NDA017799
- Marketing category
- NDA
- Marketing start
- 2005-06-08
- Marketing end
- 2022-07-08
- Substance
- DEXTROSE MONOHYDRATE; SODIUM CHLORIDE
- Active strength
- 5 g/100mL; g/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 |
|---|
| 0409-7925-09 | 00409792509 | 12 POUCH in 1 CASE (0409-7925-09) > 1 BAG in 1 POUCH > 1000 mL in 1 BAG | 12 pouch | 2006-01-09 | 2022-07-08 | No | No | Current |