NDC 55111-332 – Pantoprazole
Pantoprazole Sodium 20 mg/1 · Tablet, Delayed Release · Oral
Product NDC55111-332
Product details
- Brand name
- Pantoprazole
- Generic name
- Pantoprazole
- Labeler
- Dr.Reddy's Laboratories Limited
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA077619
- Marketed since
- January 19, 2011
- Listing expires
- December 31, 2027
- Pharmacologic class
- Proton Pump Inhibitor
Active ingredients
- Pantoprazole Sodium 20 mg/1
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 55111-332-01 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-332-01) | Jan 19, 2011 |
| 55111-332-05 | 500 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-332-05) | Jan 19, 2011 |
| 55111-332-10 | 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-332-10) | Jan 19, 2011 |
| 55111-332-30 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-332-30) | Jan 19, 2011 |
| 55111-332-78 | 10 BLISTER PACK in 1 CARTON (55111-332-78) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-332-79) | Jan 19, 2011 |
| 55111-332-81 | 3 BLISTER PACK in 1 CARTON (55111-332-81) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-332-79) | Jan 19, 2011 |
| 55111-332-90 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-332-90) | Jan 19, 2011 |
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