Pantoprazole Sodium
- Product NDC
- 72572-550
- 11-digit product format
- 725720550
- Labeler code
- 72572
- Product ID
- 72572-550_55f22a15-9d01-4ed2-863f-aaa94cb5bd54
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pantoprazole Sodium
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Civica, Inc.
- Application
- ANDA090296
- Marketing category
- ANDA
- Marketing start
- 2020-11-15
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72572-550 | PANTOPRAZOLE SODIUM INJECTION, POWDER, FOR SOLUTION [CIVICA, INC.] | 8 | Legacy NDC | 20250112_e4576dbf-0399-4860-a100-57f900095ae5.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72572-550-10 | 72572055010 | 10 VIAL in 1 CARTON (72572-550-10) > 10 mL in 1 VIAL (72572-550-01) | 10 vial | 2020-11-15 | 0000-00-00 | No | No | Current |