Pantoprazole Sodium
- Product NDC
- 55154-0777
- 11-digit product format
- 551540777
- Labeler code
- 55154
- Product ID
- 55154-0777_772ea8c7-c1b6-4d7f-94c5-5b818584f1c2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pantoprazole Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA202038
- Marketing category
- ANDA
- Marketing start
- 2015-05-01
- Marketing end
- 0000-00-00
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55154-0777-0 | 55154077700 | 10 BLISTER PACK in 1 BAG (55154-0777-0) > 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK | 10 blister pack | 2015-05-01 | 0000-00-00 | No | No | Current |