NDC 0409-7101 – Sodium Chloride
Sodium Chloride 900 mg/100mL · Injection, Solution · Intravenous
Product NDC0409-7101
Product details
- Brand name
- Sodium Chloride
- Generic name
- Sodium Chloride
- Labeler
- Hospira, Inc.
- Dosage form
- Injection, Solution
- Route
- Intravenous
- Marketing category
- NDA · NDA019465
- Marketed since
- June 30, 2005
- Marketing end
- December 31, 2026
- Pharmacologic class
- Osmotic Laxative
Active ingredients
- Sodium Chloride 900 mg/100mL
Uses, dosage, side effects and warnings for Sodium Chloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 0409-7101-02 | 24 POUCH in 1 CASE (0409-7101-02) / 1 BAG in 1 POUCH / 250 mL in 1 BAG (0409-7101-04) | Jun 30, 2005 |
| 0409-7101-67 | 10 POUCH in 1 CASE (0409-7101-67) / 5 BAG in 1 POUCH / 100 mL in 1 BAG (0409-7101-69) | Aug 24, 2005 |
Recalls mentioning this NDC
- D-0490-2015 Apr 29, 2015 · Class II
Lack of Sterility Assurance: The product has the potential to leak at the administrative port. - D-613-2013 Jul 3, 2013 · Class II
Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking bags.
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