PANTOPRAZOLE SODIUM
- Product NDC
- 55700-790
- 11-digit product format
- 557000790
- Labeler code
- 55700
- Product ID
- 55700-790_b6d9d786-7141-4371-935f-f46e54ae8822
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PANTOPRAZOLE
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA202882
- Marketing category
- ANDA
- Marketing start
- 2019-09-13
- 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
- 2023-12-31
- 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 |
|---|
| 55700-790-30 | 55700079030 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (55700-790-30) | 2019-09-13 | 0000-00-00 | No | No | Current |
| 55700-790-60 | 55700079060 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (55700-790-60) | 2019-09-13 | 0000-00-00 | No | No | Current |