Sodium Chloride
- Product NDC
- 0409-6138
- 11-digit product format
- 004096138
- Labeler code
- 0409
- Product ID
- 0409-6138_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
- 2005-05-23
- Marketing end
- 2022-08-01
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0409-6138-03 | 00409613803 | 24 BOTTLE, PLASTIC in 1 CASE (0409-6138-03) > 500 mL in 1 BOTTLE, PLASTIC | 2005-05-23 | 2022-08-01 | No | No | Current |
| 0409-6138-22 | 00409613822 | 24 BOTTLE, PLASTIC in 1 CASE (0409-6138-22) > 250 mL in 1 BOTTLE, PLASTIC | 2005-08-11 | 2022-08-01 | No | No | Current |