NDC 0409-7332 – Ceftriaxone Sodium
Ceftriaxone Sodium 1 g/1 · Injection, Powder, For Solution · Intramuscular, Intravenous
Product NDC0409-7332
Product details
- Brand name
- Ceftriaxone Sodium
- Generic name
- Ceftriaxone Sodium
- Labeler
- Hospira, Inc
- Dosage form
- Injection, Powder, For Solution
- Route
- Intramuscular, Intravenous
- Marketing category
- ANDA · ANDA065169
- Marketed since
- May 9, 2005
- Listing expires
- December 31, 2027
- Pharmacologic class
- Cephalosporin Antibacterial
Active ingredients
- Ceftriaxone Sodium 1 g/1
Uses, dosage, side effects and warnings for Ceftriaxone Sodium →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 0409-7332-01 | 10 VIAL, SINGLE-USE in 1 CARTON (0409-7332-01) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE (0409-7332-11) | May 9, 2005 |
| 0409-7332-20 | 10 VIAL, SINGLE-USE in 1 CARTON (0409-7332-20) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE (0409-7332-21) | Mar 19, 2018 |
Recalls mentioning this NDC
- D-0145-2017 Nov 30, 2016 · Class III
Labeling: Missing Label
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