Pantoprazole Sodium
- Product NDC
- 66993-067
- 11-digit product format
- 669930067
- Labeler code
- 66993
- Product ID
- 66993-067_b0b07f99-598e-44d0-b276-f0e8b010df5e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pantoprazole Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Prasco Laboratories
- Application
- ANDA202038
- Marketing category
- ANDA
- Marketing start
- 2015-05-01
- Marketing end
- 2022-10-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 66993-067-80 | 66993006780 | 10 BLISTER PACK in 1 CARTON (66993-067-80) > 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (66993-067-51) | 10 blister pack | 2015-05-01 | 2022-10-31 | No | No | Current |
| 66993-067-85 | 66993006785 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (66993-067-85) | | 2015-05-01 | 2022-10-31 | No | No | Current |