NDC 31722-713 – Pantoprazole Sodium
Pantoprazole Sodium 40 mg/1 · Tablet, Delayed Release · Oral
Product NDC31722-713
Product details
- Brand name
- Pantoprazole Sodium
- Generic name
- Pantoprazole
- Labeler
- Camber Pharmaceuticals, Inc.
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA202882
- Marketed since
- September 10, 2014
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 31722-713-10 | 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (31722-713-10) | Sep 10, 2014 |
| 31722-713-31 | 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (31722-713-31) | Sep 10, 2014 |
| 31722-713-32 | 10 TABLET, DELAYED RELEASE in 1 CARTON (31722-713-32) | Sep 10, 2014 |
| 31722-713-90 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (31722-713-90) | Sep 10, 2014 |
Recalls mentioning this NDC
- D-0484-2026 Apr 29, 2026 · Class II
Discoloration: Firm received five (5) complaints stating that, "Tablets discolored darker than normal and have lighter-colored spots." - D-0530-2023 Apr 19, 2023 · Class II
CGMP Deviations: Discoloration
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