Sodium Chloride
- Product NDC
- 0409-7138
- 11-digit product format
- 004097138
- Labeler code
- 0409
- Product ID
- 0409-7138_e4989da2-308c-44cc-9b49-1fb841da6f12
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SODIUM CHLORIDE
- Dosage form
- IRRIGANT
- Route
- IRRIGATION
- Labeler
- Hospira, Inc.
- Application
- NDA017514
- Marketing category
- NDA
- Marketing start
- 2005-05-13
- Marketing end
- 2022-07-01
- Substance
- SODIUM CHLORIDE
- Active strength
- 900 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
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0409-7138-09 | 00409713809 | 12 BOTTLE, PLASTIC in 1 CASE (0409-7138-09) > 1000 mL in 1 BOTTLE, PLASTIC | 2005-05-13 | 2022-07-01 | No | No | Current |
| 0409-7138-36 | 00409713836 | 9 BOTTLE, PLASTIC in 1 CASE (0409-7138-36) > 1500 mL in 1 BOTTLE, PLASTIC | 2005-06-02 | 2021-12-01 | No | No | Current |