NDC 65219-385 – Pantoprazole Sodium
Pantoprazole Sodium 40 mg/10mL · Injection, Powder, Lyophilized, For Solution · Intravenous
Product NDC65219-385
Product details
- Brand name
- Pantoprazole Sodium
- Generic name
- Pantoprazole Sodium
- Labeler
- Fresenius Kabi USA, LLC
- Dosage form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Marketing category
- ANDA · ANDA216021
- Marketed since
- August 1, 2024
- Listing expires
- December 31, 2026
- Pharmacologic class
- Proton Pump Inhibitor
Active ingredients
- Pantoprazole Sodium 40 mg/10mL
Uses, dosage, side effects and warnings for Pantoprazole Sodium →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 65219-385-10 | 10 VIAL in 1 CARTON (65219-385-10) / 10 mL in 1 VIAL (65219-385-01) | Jan 31, 2025 |
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