Pantoprazole Sodium
- Product NDC
- 55154-4330
- 11-digit product format
- 551544330
- Labeler code
- 55154
- Product ID
- 55154-4330_53dacfcf-c266-485b-ae0b-8fddc93f1b6a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pantoprazole Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA078281
- Marketing category
- ANDA
- Marketing start
- 2013-01-23
- Marketing end
- 0000-00-00
- Substance
- PANTOPRAZOLE SODIUM
- Active strength
- 20 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 |
|---|
| 55154-4330-0 | 55154433000 | 10 BLISTER PACK in 1 BAG (55154-4330-0) > 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK | 10 blister pack | 2013-01-23 | 0000-00-00 | No | No | Current |