Pantoprazole Sodium
- Product NDC
- 50090-1850
- 11-digit product format
- 500901850
- Labeler code
- 50090
- Product ID
- 50090-1850_b3fbd7cb-3597-4593-8efb-985125a3be93
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pantoprazole Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA090074
- Marketing category
- ANDA
- Marketing start
- 2011-01-20
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-1850-0 | 50090185000 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-1850-0) | 2015-05-29 | 0000-00-00 | No | No | Current |
| 50090-1850-1 | 50090185001 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-1850-1) | 2015-05-29 | 0000-00-00 | No | No | Current |
| 50090-1850-2 | 50090185002 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-1850-2) | 2018-08-08 | 0000-00-00 | No | No | Current |