Pantoprazole Sodium
- Product NDC
- 55700-329
- 11-digit product format
- 557000329
- Labeler code
- 55700
- Product ID
- 55700-329_3b76fd13-1aba-494d-93fc-ed90fac21456
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pantoprazole Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA078281
- Marketing category
- ANDA
- Marketing start
- 2018-02-27
- 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
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 55700-329-30 | 2025-01-08 | C162847 | 48780-1 | ba0f9c33-190a-a910-e053-dadaa90a0b85 | f849318e-e209-4693-bf1d-c7bf98f3f341 |
| 55700-329-60 | 2025-01-08 | C162847 | 48780-1 | ba0f9c33-190a-a910-e053-dadaa90a0b85 | f849318e-e209-4693-bf1d-c7bf98f3f341 |
| 55700-329-30 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-190a-a910-e053-dadaa90a0b85 | f849318e-e209-4693-bf1d-c7bf98f3f341 |
| 55700-329-60 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-190a-a910-e053-dadaa90a0b85 | f849318e-e209-4693-bf1d-c7bf98f3f341 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 55700-329-30 | EA - Each | 55700-329 | bd4fe8cb-9317-4e90-85d4-f5224c317c1a | 1 | 2018-04-19 |
| 55700-329-60 | EA - Each | 55700-329 | a71ee92d-07c6-4477-ab5a-efc6dfe8a417 | 1 | 2018-04-19 |