PANTOPRAZOLE SODIUM
- Product NDC
- 70332-300
- 11-digit product format
- 703320300
- Labeler code
- 70332
- Product ID
- 70332-300_55eebe36-e733-5c58-e054-00144ff8d46c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PANTOPRAZOLE
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- California Pharmaceuticals LLC
- Application
- ANDA205119
- Marketing category
- ANDA
- Marketing start
- 2017-07-01
- Marketing end
- 0000-00-00
- Substance
- PANTOPRAZOLE SODIUM
- Active strength
- 40 mg/1
- Pharmacologic classes
- Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70332-300-01 | PANTOPRAZOLE SODIUM | 7 in 1 BOTTLE | TABLET, DELAYED RELEASE | 7 | | 3 |
| 70332-300-02 | PANTOPRAZOLE SODIUM | 30 in 1 BOTTLE | TABLET, DELAYED RELEASE | 30 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70332-300 | PANTOPRAZOLE SODIUM (PANTOPRAZOLE) TABLET, DELAYED RELEASE [CALIFORNIA PHARMACEUTICALS LLC] | 3 | Legacy NDC, 2 package rows | 20170804_962951c7-1467-49f7-9ada-361e86fdfcb2.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 70332-300-01 | 70332030001 | 7 in 1 BOTTLE | Historical |
| 70332-300-02 | 70332030002 | 30 in 1 BOTTLE | Historical |