Pantoprazole Sodium
- Product NDC
- 63187-974
- 11-digit product format
- 631870974
- Labeler code
- 63187
- Product ID
- 63187-974_ed77dc17-564e-44a4-810b-44952cda19e3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pantoprazole
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA205119
- Marketing category
- ANDA
- Marketing start
- 2016-06-20
- Substance
- PANTOPRAZOLE SODIUM
- Active strength
- 40 mg/1
- Pharmacologic classes
- Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 6871619Q5X | PANTOPRAZOLE SODIUM | 164579-32-2 | PANTOPRAZOLE SODIUM |
| D8TST4O562 | PANTOPRAZOLE | 102625-70-7 | Pantoprazole |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 63187-974-30 | 63187097430 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-974-30) | 2016-06-20 | No | No | Historical |
| 63187-974-60 | 63187097460 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-974-60) | 2016-06-20 | No | No | Historical |
| 63187-974-90 | 63187097490 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-974-90) | 2016-06-20 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Pantoprazole Sodium | Proficient Rx LP | 2019-11-01 | HUMAN PRESCRIPTION DRUG LABEL | 3 |