Rabeprazole Sodium
- Product NDC
- 72162-2367
- 11-digit product format
- 721622367
- Labeler code
- 72162
- Product ID
- 72162-2367_52e17eb4-6cf4-4516-a04b-2859262f7fbb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Rabeprazole Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA208644
- Marketing category
- ANDA
- Marketing start
- 2018-04-27
- Substance
- RABEPRAZOLE SODIUM
- Active strength
- 20 mg/1
- Pharmacologic classes
- Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Rabeprazole Sodium
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| RABEPRAZOLE SODIUM | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3L36P16U4R |
| Rxcui | 854868 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-2367-5 | Rabeprazole Sodium | 500 in 1 BOTTLE | TABLET, DELAYED RELEASE | 500 | | 100 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-2367 | RABEPRAZOLE SODIUM TABLET, DELAYED RELEASE [BRYANT RANCH PREPACK] | 100 | Current NDC, 1 package rows | 20240718_8d8c1a72-b4c4-4699-b9c3-3a39a9df44f2.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2367-5 | 72162236705 | 500 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2367-5) | 2024-07-16 | No | No | Historical |