Sodium Chloride
- Product NDC
- 0409-7972
- 11-digit product format
- 004097972
- Labeler code
- 0409
- Product ID
- 0409-7972_e4989da2-308c-44cc-9b49-1fb841da6f12
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SODIUM CHLORIDE
- Dosage form
- IRRIGANT
- Route
- IRRIGATION
- Labeler
- Hospira, Inc.
- Application
- NDA018314
- Marketing category
- NDA
- Marketing start
- 2005-03-28
- Marketing end
- 2022-07-08
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0409-7972-07 | 00409797207 | 6 BAG in 1 CASE (0409-7972-07) > 2000 mL in 1 BAG | 6 bag | 2005-03-28 | 2022-07-08 | No | No | Current |
| 0409-7972-08 | 00409797208 | 4 POUCH in 1 CASE (0409-7972-08) > 1 BAG in 1 POUCH > 3000 mL in 1 BAG | 4 pouch | 2005-05-10 | 2021-05-01 | No | No | Current |