Pantoprazole Sodium
- Product NDC
- 60760-151
- 11-digit product format
- 607600151
- Labeler code
- 60760
- Product ID
- 60760-151_7acba366-852c-cba6-e053-2a91aa0a9980
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pantoprazole Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-151-60 | 60760015160 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-151-60) | 2011-01-20 | 0000-00-00 | No | No | Current |