NDC 55150-202 – Pantoprazole Sodium
Pantoprazole Sodium 40 mg/1 · Injection, Powder, For Solution · Intravenous
Product NDC55150-202
Product details
- Brand name
- Pantoprazole Sodium
- Generic name
- Pantoprazole Sodium
- Labeler
- Eugia US LLC
- Dosage form
- Injection, Powder, For Solution
- Route
- Intravenous
- Marketing category
- ANDA · ANDA205675
- Marketed since
- March 30, 2016
- Listing expires
- December 31, 2027
- Pharmacologic class
- Proton Pump Inhibitor
Active ingredients
- Pantoprazole Sodium 40 mg/1
Uses, dosage, side effects and warnings for Pantoprazole Sodium →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 55150-202-10 | 10 VIAL, SINGLE-DOSE in 1 CARTON (55150-202-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (55150-202-00) | Mar 30, 2016 |
| 55150-202-25 | 25 VIAL, SINGLE-DOSE in 1 CARTON (55150-202-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (55150-202-00) | Mar 30, 2016 |
Recalls mentioning this NDC
- D-0340-2018 Feb 14, 2018 · Class I
Presence of Particulate Matter: One vial from a lot of Pantoprazole Sodium for Injection (40 mg) contained a piece of glass - D-0470-2017 Feb 15, 2017 · Class III
Discoloration: Some vials were found to contain powder with a yellowish-brownish appearance.
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