NDC 76420-671 – Pantoprazole Sodium
Pantoprazole Sodium 20 mg/1 · Tablet, Delayed Release · Oral
Product NDC76420-671
Product details
- Brand name
- Pantoprazole Sodium
- Generic name
- Pantoprazole
- Labeler
- Asclemed USA, Inc.
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA202882
- Marketed since
- September 10, 2014
- Listing expires
- December 31, 2026
- Pharmacologic class
- Proton Pump Inhibitor
Active ingredients
- Pantoprazole Sodium 20 mg/1
Uses, dosage, side effects and warnings for Pantoprazole Sodium →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 76420-671-01 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-671-01) | Mar 13, 2024 |
| 76420-671-10 | 10 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-671-10) | Mar 13, 2024 |
| 76420-671-30 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-671-30) | Mar 13, 2024 |
| 76420-671-60 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-671-60) | Mar 13, 2024 |
| 76420-671-90 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-671-90) | Mar 13, 2024 |
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