Pantoprazole Sodium
- Product NDC
- 0480-4111
- 11-digit product format
- 004804111
- Labeler code
- 0480
- Product ID
- 0480-4111_4a6fc900-88af-4684-814d-2e93437b613b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pantoprazole Sodium
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Application
- ANDA090296
- Marketing category
- ANDA
- Marketing start
- 2022-09-09
- Marketing end
- 0000-00-00
- Substance
- PANTOPRAZOLE SODIUM
- Active strength
- 40 mg/10mL
- Pharmacologic classes
- Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 0480-4111-03 | 00480411103 | 10 VIAL in 1 CARTON (0480-4111-03) > 10 mL in 1 VIAL (0480-4111-01) | 10 vial | 2022-09-09 | 0000-00-00 | No | No | Current |